Polypeptides targeting HIV fusion

ABSTRACT

The invention is directed to polypeptides comprising a CD4 binding moiety, a gp41 binding moiety, a HIV fusion peptide inhibitor moiety and combinations thereof. More specifically, the present invention relates to polypeptides comprising a fibronectin-based scaffold domain protein that binds CD4, a fibronectin-based scaffold domain protein that binds the N17 domain of gp41, and a HIV fusion peptide inhibitor or combinations thereof. The invention also relates to the use of the innovative proteins in therapeutic applications to treat HIV.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No. 15/568,830, filed on 24 Oct. 2017, now U.S. Pat. No. 10,407,490, which is a 371 of lntemational PCT/US2016/027424 filed on 14 Apr. 2016, which claims priority to U.S. Provisional Application Ser. Nos. 62/152,271, filed Apr. 24, 2015, and 62/257,474, filed Nov. 19, 2015; the entire contents of which are incorporated herein by reference.

FIELD OF THE INVENTION

The invention is directed to polypeptides comprising a CD4 binding moiety, a gp41 binding moiety, a HIV fusion peptide inhibitor moiety and combinations thereof. More specifically, the present invention relates to polypeptides comprising a fibronectin-based scaffold domain protein that binds CD4, a fibronectin-based scaffold domain protein that binds the N17 domain of gp41, and a HIV fusion peptide inhibitor or combinations thereof. The invention also relates to the use of the innovative proteins in therapeutic applications to treat HIV.

BACKGROUND OF THE INVENTION

Acquired immunodeficiency syndrome (AIDS) is the result of infection by the retrovirus known as human immunodeficiency virus (HIV). It remains a major medical problem, with an estimated 35 million people infected worldwide at the end of 2013. During that year, there were 2.1 million new infections, with 1.5 million people dying from complications due to AIDS.

Current therapy for HIV-infected individuals consists of a combination of approved anti-retroviral agents. Over two dozen drugs are currently approved for HIV infection, either as single agents, fixed dose combinations or single tablet regimens, the latter two containing 2-4 approved agents. These agents belong to a number of different classes, targeting either a viral enzyme or the function of a viral protein during the virus life cycle. Thus, agents are classified as either nucleotide reverse transcriptase inhibitors (NRTIs), non-nucleotide reverse transcriptase inhibitors (NNRTIs), protease inhibitors (PIs), integrase inhibitors (INIs), or entry inhibitors (one entry inhibitor, maraviroc, targets the host CCR5 protein, while the other, enfuvirtide, is a peptide that targets the gp41 region of the viral gp160 protein). In addition, a pharmacokinetic enhancer with no antiviral activity (cobicistat) has been approved for use in combinations with antiretroviral agents (ARVs) that require boosting.

Despite the armamentarium of agents and drug combinations, there remains a medical need for new anti-retroviral agents, due in part to the need for chronic dosing to combat infection. Significant problems related to long-term toxicities are documented, creating a need to address and prevent these co-morbidities (e.g., CNS, CV/metabolic, renal disease). Also, increasing failure rates on current therapies continue to be a problem, due either to the presence or emergence of resistant strains or to non-compliance attributed to drug holidays or adverse side effects. For example, despite therapy, it has been estimated that 63% of subjects receiving combination therapy remained viremic, as they had viral loads>500 copies/ml (Oette, M. et al., “Primary HIV Drug Resistance and Efficacy of First-Line Antiretroviral Therapy Guided by Resistance Testing”, J. Acq. Imm. Def. Synd., 41(5):573-581 (2006)). Among these patients, 76% had viruses that were resistant to one or more classes of antiretroviral agents. As a result, new drugs are needed that are more convenient, have high genetic barriers to the development of resistance and have improved safety over current agents.

It is now well known that cells can be infected by HIV through a process by which fusion occurs between the cellular membrane and the viral membrane. The generally accepted model of this process is that the viral envelope glycoprotein complex (gp120/gp41) interacts with cell surface receptors on the membranes of the target cells. Following binding of gp120 to cellular receptors (e.g., CD4 in combination with a chemokine co-receptor such as CCR5 or CXCR4), a conformational change is induced in the gp120/gp41 complex that allows gp41 to insert into the membrane of the target cell and mediate membrane fusion. As these entry processes occur on the cell membrane, they are amenable for inhibition by macrocmolecules, which include biologic peptides (Haqqani et al., Antiviral Res., 98:158 (2013)). For instance, the approved antiviral peptide enfuvirtide (FUZEON®) targets a region of gp41 involved in membrane fusion. Larger polypeptides such as monoclonal antibodies can also inhibit different aspects of virus entry. A monoclonal antibody targeting the first step of virus entry, interaction with the cellular receptor CD4 (ibalizumab; Bruno et al., J. Antimicrob. Chemother., 65:1839 (2010)), as well as a monoclonal antibody targeting the co-receptor CCR5 (PRO-140; Tenorio, Curr. HIV/AIDS Rep., 8:1 (2011)) have both shown positive results in Phase 2a trials. These antibodies also have the property of being long acting antiretrovirals, with potential dosing regimens of weekly to monthly (Jacobson et al., J. Infect. Dis., 201:1481 (2010); Jacobson et al., Antimicrob. Agents Chemother., 53:450 (2009)).

Another property of peptide entry inhibitors is that enhanced or synergistic potency can be obtained if two peptide inhibitors are attached to each other, or if a single inhibitor is localized near the site of action through binding to membrane biomolecules. Thus, attaching a fusion peptide inhibitor to a monoclonal antibody targeting CCR5 (Kopetzki et al., Virol. J., 5:56 (2008)) or attaching a cholesterol moiety to the C-terminus of a peptide fusion inhibitor to place it at the surface of the target cell membrane (Ingallinela et al., Proc. Natl. Acad. Sci. USA, 106:5801 (2009); Augusto et al., J. Antimicrob. Chemother., 69:1286 (2014)) drastically increases the potency of the combined molecule compared to the separate molecules. Similarly, bispecific antibodies consisting of anti-HIV-1 neutralizing antibody fragments targeting gp120 fused to ibalizumab showed synergistic increases in potency compared to the individual inhibitors (Sun et al., J. Acquir. Immune Defic. Syndr., 66:473 (2014)). The Combinectin molecules of the invention makes use of these various properties.

SUMMARY OF THE INVENTION

The invention is directed to polypeptides comprising a CD4 binding moiety, a gp41 binding moiety, a HIV fusion peptide inhibitor moiety and combinations thereof.

One embodiment of the invention is directed to polypeptides comprising a fibronectin-based scaffold domain protein that binds CD4, a fibronectin-based scaffold domain protein that binds the N17 domain of gp41, and a HIV fusion peptide inhibitor.

In one embodiment of the invention, the three domains are connected to each other by linkers. In another embodiment of the invention, the three domains may be connected to each other in any order. In another embodiment of the invention, the polypeptide comprises an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the non-linker regions of SEQ ID NO: 3, 5, 7 or 9.

The invention is also directed to polypeptides comprising a fibronectin-based scaffold domain protein that binds CD4 and a fibronectin-based scaffold domain protein that binds the N17 domain of gp41. In one embodiment of the invention, the two domains are connected to each other by linkers. In another embodiment of the invention, the two domains may be connected to each other in any order.

The invention is also directed to polypeptides comprising a fibronectin-based scaffold domain protein that binds CD4 and a HIV fusion peptide inhibitor. In one embodiment of the invention, the two domains are connected to each other by linkers. In another embodiment of the invention, the two domains may be connected to each other in any order.

The invention is also directed to polypeptides comprising a fibronectin-based scaffold domain protein that binds the N17 domain of gp41, and a HIV fusion peptide inhibitor. In one embodiment of the invention, the two domains are connected to each other by linkers. In another embodiment of the invention, the two domains may be connected to each other in any order. In another embodiment of the invention, the polypeptide comprises an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the non-linker regions of SEQ ID NO: 410-428.

Another embodiment of the invention is also directed to polypeptides comprising three active domains, a fibronectin-based scaffold domain protein that binds CD4, a gp41 binding moiety and a HIV fusion peptide inhibitor moiety. The invention is also directed to polypeptides comprising a fibronectin-based scaffold domain protein that binds gp41, a CD4 binding moiety and a HIV fusion peptide inhibitor moiety. The invention is also directed to polypeptides comprising a CD4 binding moiety, a gp41 binding moiety and a HIV fusion peptide inhibitor. In one embodiment of the invention, the two domains are connected to each other by linkers. In another embodiment of the invention, the two domains may be connected to each other in any order.

The invention is also directed to polypeptides comprising two active domains, a fibronectin-based scaffold domain protein that binds CD4 and a gp41 binding moiety. The invention is also directed to polypeptides comprising a fibronectin-based scaffold domain protein that binds gp41 and a CD4 binding moiety. The invention is also directed to polypeptides comprising a CD4 binding moiety and a HIV fusion peptide inhibitor. The invention is also directed to polypeptides comprising a gp41 binding moiety and a HIV fusion peptide inhibitor. In one embodiment of the invention, the two domains are connected to each other by linkers. In another embodiment of the invention, the two domains may be connected to each other in any order.

Another embodiment of the invention is also directed to anti-CD4 Adnectin™ anti-N17 Adnectin™, or HIV fusion peptide inhibitors. In another embodiment of the invention, the polypeptide comprises an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the non-linker regions of SEQ ID NO: 95-114 or SEQ ID NO: 115-371 or SEQ ID NO: 372-392, respectively.

In another embodiment of the invention, a pharmacokinetic (PK) moiety is attached to the polypeptides of the invention. Examples of a PK moiety include but are not limited to polyethylene glycol, sialic acid, Fc, Fc fragment, transferrin, serum albumin (HSA), a serum albumin binding protein, and a serum immunoglobulin binding protein. In one embodiment of the invention, the PK moiety may be attached to the linker regions, or the N- or C-terminus of the polypeptide of the invention. In another embodiment of the invention, the polypeptide comprises an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the non-linker regions of SEQ ID NO: 4, 6, 8 or 10.

The invention is also directed to a polypeptide comprising the amino acid sequence of any one of the sequences shown in SEQ ID NO: 3-10.

The invention is also directed to a pharmaceutical composition comprising one or more of the polypeptides of the invention and a carrier.

The invention also provides a method of treating HIV in a subject comprising administering an effective amount of the polypeptides of the invention.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a diagram of alternative Combinectins. One of the Adnectin™ binds CD4, a second Adnectin™ binds the HR1 region of gp41. The peptide also binds in the HR1 region of gp41. The different components of the Combinectin are connected to each other in any order by linkers. Any of the Combinectins may have a PK moiety attached, such as HSA or Fc.

FIG. 2 shows the amino acid sequences of Fc fusion-Combinectin 3137_(SEQ ID NO:4), 3151_(SEQ ID NO:6) and human serum albumin (HSA) fusion-Combinectin 3191_(SEQ ID NO:8), and 3202_(SEQ ID NO:10). The Fc and HSA sequences are in bold. The anti-CD4 Adnectin sequences are underlined. The anti-N17 Adnectin sequences are double underlined. The HIV inhibitor peptide sequences are underlined in bold. The linker sequences are italicized.

FIG. 3 shows the potency (EC₅₀ and EC₉₀) of Combinectin 3137, 3151, 3191 and 3202, as described in Example 2.

FIG. 4 shows the PK properties of Combinectin 3137, 3151, 3191 and 3202 as described in Example 3.

FIG. 5 shows the amino acid sequences of anti-N17 Adnectin™ in combination with an HIV fusion peptide inhibitor, which correspond to the sequences described in Table 4 minus the N-terminus and C-terminus extended regions. The anti-N17 Adnectin™ sequences are double underlined. The HIV fusion peptide inhibitor sequences are underlined in bold. The linker sequences are italicized.

FIG. 6 shows the WebLogo for the CD loop of anti-CD4 Adnectin™. WebLogo generates sequence logos, graphical representations of the patterns within a multiple sequence alignment. Each logo consists of stacks of letters, one stack for each position in the sequence. The overall height of each stack indicates the sequence conservation at that position (measured in bits), whereas the height of symbols within the stack reflects the relative frequency of the corresponding amino or nucleic acid at that position (Crooks, G. E. et al., “WebLogo: A sequence logo generator”, Genome Research, 14:1188-1190 (2004)).

FIG. 7 shows the WebLogo for the FG loop of anti-CD4 Adnectin™ (Schneider, T. D. et al., “Sequence Logos: A New Way to Display Consensus Sequences”, Nucleic Acids Res., 18:6097-6100 (1990)).

FIG. 8 shows point mutation data for the HIV fusion peptide inhibitor. The aspartic acid (D) near the C-terminus of the HIV fusion peptide inhibitor was replaced with the amino acids listed along the x axis.

DETAILED DESCRIPTION OF THE INVENTION Definitions

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by the skilled artisan. Although any methods and compositions similar or equivalent to those described herein can be used in practice or testing of the present invention, the preferred methods and compositions are described herein.

“Polypeptide” as used herein refers to any sequence of two or more amino acids, regardless of length, post-translation modification, or function. “Polypeptide”, “peptide”, and “protein” are used interchangeably herein. Polypeptides can be modified in any of a variety of standard chemical ways (e.g., an amino acid can be modified with a protecting group; the carboxy-terminal amino acid can be made into a terminal amide group; the amino-terminal residue can be modified with groups to, e.g., enhance lipophilicity; or the polypeptide can be chemically glycosylated or otherwise modified to increase stability or in vivo half-life). Polypeptide modifications can include the attachment of another structure such as a cyclic compound or other molecule to the polypeptide and can also include polypeptides that contain one or more amino acids in an altered configuration (i.e., R or S; or, L or D).

The peptides of the invention may include, for example, proteins derived from the tenth type III domain of fibronectin that have been modified to bind to CD4 or N17 domain of gp41 and are referred to herein as, “anti-CD4 Adnectin™”, “anti-N17 Adnectin™”, “CD4 Adnectin™” or “gp41 Adnectin™”. The polypeptides of the invention may also include peptides modeled after the heptad repeat 2 (HR2) region of HIV envelope glycoprotein gp41, which inhibit fusion by binding the heptad repeat 1 (HR1) region of gp41 and are referred to herein as “HIV fusion peptide inhibitor” or “fusion peptide inhibitor”. The polypeptides of the invention also include “Combinectins” comprising an anti-CD4 Adnectin™ linked to an anti-N17 Adnectin™ linked to a HIV fusion peptide inhibitor (FIG. 1). Alternatively, the Combinectin comprises an anti-CD4 Adnectin™ linked to an anti-N17 Adnectin™ or an anti-N17 Adnectin™ linked to a HIV fusion peptide inhibitor or an anti-CD4 Adnectin™ linked to a HIV fusion peptide inhibitor.

A “polypeptide chain”, as used herein, refers to a polypeptide wherein each of the domains thereof is joined to other domain(s) by peptide bond(s), as opposed to non-covalent interactions or disulfide bonds.

An “isolated” polypeptide is one that has been identified and separated and/or recovered from a component of its natural environment. Contaminant components of its natural environment are materials that would interfere with diagnostic or therapeutic uses for the polypeptide, and may include recombinant host cell proteins and other proteinaceous or nonproteinaceous solutes. In one embodiment, the polypeptides will be purified (1) to greater than 95% by weight of polypeptide as determined by the Lowry method, and most preferably more than 99% by weight, or (2) to homogeneity by SDS-PAGE under reducing or nonreducing condition using Coomassie blue or, silver stain. Ordinarily, isolated polypeptide will be prepared by at least one purification step.

“Percent (%) amino acid sequence identity” herein is defined as the percentage of amino acid residues in a candidate sequence that are identical with the amino acid residues in a selected sequence, after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent sequence identity, and not considering any conservative substitutions as part of the sequence identity. Alignment for purposes of determining percent amino acid sequence identity can be achieved in various ways that are within the skill in the art, for instance, using publicly available computer software such as BLAST, BLAST-2, ALIGN, ALIGN-2 or Megalign (DNASTAR®) software. Those skilled in the art can readily determine appropriate parameters for measuring alignment, including any algorithms needed to achieve maximal alignment over the full-length of the sequences being compared. For example, the % amino acid sequence identity of a given amino acid sequence A to, with, or against a given amino acid sequence B (which can alternatively be phrased as a given amino acid sequence A that has or comprises a certain % amino acid sequence identity to, with, or against a given amino acid sequence B) is calculated as follows: 100 times the fraction X/Y where X is the number of amino acid residues scored as identical matches by the sequence alignment program ALIGN-2 in that program's alignment of A and B, and where Y is the total number of amino acid residues in B. It will be appreciated that where the length of amino acid sequence A is not equal to the length of amino acid sequence B, the % amino acid sequence identity of A to B will not equal the % amino acid sequence identity of B to A.

As used herein, “conservative substitution” denotes the replacement of an amino acid residue by another, without altering the overall conformation and function of the peptide, including, but not limited to, replacement of an amino acid with one having similar properties (such as, for example, polarity, hydrogen bonding potential, acidic, basic, shape, hydrophobic, aromatic, and the like). Amino acids with similar properties are well known in the art. For example, arginine, histidine and lysine are hydrophilic-basic amino acids and may be interchangeable. Similarly, isoleucine, a hydrophobic amino acid, may be replaced with leucine, methionine or valine. Neutral hydrophilic amino acids, which can be substituted for one another, include asparagine, glutamine, serine and threonine. By “substituted” or “modified” the present invention includes those amino acids that have been altered or modified from naturally occurring amino acids. As such it should be understood that in the context of the present invention a conservative substitution is recognized in the art as a substitution of one amino acid for another amino acid that has similar properties.

As used herein, the term “binding site” refers to the site or portion of a protein (e.g., CD4, gp41) that interacts or binds to a particular protein of the invention (e.g., as an epitope is recognized by an antibody). Binding sites can be formed from contiguous amino acids or noncontiguous amino acids juxtaposed by tertiary folding of a protein. Binding sites formed by contiguous amino acids are typically retained on exposure to denaturing solvents, whereas binding sites formed by tertiary folding are typically lost on treatment of denaturing solvents.

The binding site for an anti-CD4 moiety or anti-N17moiety of the invention may be determined by application of standard techniques typically used for epitope mapping of antibodies including, but not limited to protease mapping and mutational analysis. Alternatively, a binding site can be determined by competition assay using a reference protein (e.g., another Adnectin™ or antibody) which binds to the same polypeptide, e.g., CD4 or gp41. If the test protein and reference molecule (e.g., another Adnectin™ or antibody) compete, then they bind to the same binding site or to binding sites sufficiently proximal such that binding of one molecule interferes with the other.

The terms “specifically binds”, “specific binding”, “selective binding”, and “selectively binds”, as used interchangeably herein refers to a protein that exhibits affinity for a CD4 or gp41, but does not significantly bind (e.g., less than about 10% binding) to a different polypeptide as measured by a technique available in the art such as, but not limited to, Scatchard analysis and/or competitive binding assays (e.g., competition ELISA, BIACORE® SPR assay). The term is also applicable where e.g., a binding domain of a protein of the invention is specific for CD4 or gp41.

The term “preferentially binds” as used herein refers to the situation in which the peptides of the invention bind CD4 or gp41 at least about 20% greater than it binds a different polypeptide as measured by a technique available in the art such as, but not limited to, Scatchard analysis and/or competitive binding assays (e.g., competition ELISA, BIACORE® SPR assay).

As used herein, the term “cross-reactivity” refers to a protein which binds to more than one distinct protein having identical or very similar binding sites.

The term “K_(d)”, as used herein, is intended to refer to the dissociation equilibrium constant of a particular Adnectin™-protein, fusion peptide inhibitor-protein or Combinectin-protein (e.g., CD4 and/or gp41) interaction or the affinity of an Adnectin™ fusion peptide inhibitor or Combinectin for a protein (e.g., CD4 and/or gp41), as measured using a surface plasmon resonance assay or a cell binding assay. A “desired K_(d)”, as used herein, refers to a K_(d) of a protein of the invention that is sufficient for the purposes contemplated. For example, a desired K_(d) may refer to the K_(d) of a Combinectin required to elicit a functional effect in an in vitro assay, e.g., a cell-based luciferase assay.

The term “k_(on)”, as used herein, is intended to refer to the association rate constant for the association of, for example, a Combinectin into the Combinectin/protein complex.

The term “k_(off)”, as used herein, is intended to refer to the dissociation rate constant for the dissociation of, for example, a Combinectin from the Combinectin/protein complex.

The term “IC₅₀”, as used herein, refers to the concentration of, for example, a Combinectin that inhibits a response, either in an in vitro or an in vivo assay, to a level that is 50% of the maximal inhibitory response, i.e., halfway between the maximal inhibitory response and the untreated response.

The terms “inhibit” or “neutralize” as used herein with respect to an activity of a protein of the invention means the ability to substantially antagonize, prohibit, prevent, restrain, slow, disrupt, eliminate, stop, reduce or reverse e.g., progression or severity of that which is being inhibited including, but not limited to, a biological activity or property, a disease or a condition. The inhibition or neutralization is preferably at least about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or higher.

The term “PK” is an acronym for “pharmacokinetic” and encompasses properties of a compound including, by way of example, absorption, distribution, metabolism, and elimination by a subject. A “PK modulation protein” or “PK moiety” as used herein refers to any protein, peptide, or moiety that affects the pharmacokinetic properties of a biologically active molecule when fused to or administered together with the biologically active molecule. Examples of a PK modulation protein or PK moiety include PEG, human serum albumin (HSA) binders (as disclosed in U.S. Publication No. 2005/0287153, U.S. Pat. No. 7,696,320, PCT Publication Nos. WO 2009/083804 and WO 2009/133208), human serum albumin, Fc or Fc fragments and variants thereof, and sugars (e.g., sialic acid).

The term “CD4 binding moiety” refers to any moiety that blocks HIV surface protein gp120 binding to the CD4 receptor on CD4+ T cells. The CD4 binding moiety may be anti-CD4-Adnectin™, -antibody (such as ibalizumab), -domain antibody (dAb), -antibody fragments (Fab), -bispecific antibody and fusion protein thereof.

The term “gp41 binding moiety” refers to any moiety that interferes with the interaction of the viral envelope glycoprotein complex (gp120/gp41) with T cells. The gp41 binding moiety may be anti-gp41-Adnectin™, -antibody (Ab), -domain antibody (dAb), -antibody fragments (Fab), -bispecific antibody and fusion protein thereof.

A “HIV fusion peptide inhibitor moiety” refers to any moiety that inhibits fusion by binding the heptad repeat 1 (HR1) region of gp41. Examples of fusion peptide inhibitor moiety include peptides derived from the NHR and CHR regions of gp41, designated NHR and CHR peptides, respectively. Enfuvirtide is an example of a CHR peptide.

The peptides of the invention may include, for example, the CD4 monoclonal antibody ibalizumab, an anti-N17 Adnectin™ and a HIV fusion peptide inhibitor. Alternatively, the peptides of the invention may include an anti-CD4 Adnectin™, an anti-N17 Adnectin™ and the HIV fusion peptide inhibitor enfuvirtide.

The “half-life” of an amino acid sequence or compound can generally be defined as the time taken for the serum concentration of the polypeptide to be reduced by 50%, in vivo, for example, due to degradation of the sequence or compound and/or clearance or sequestration of the sequence or compound by natural mechanisms. The half-life can be determined in any manner known per se, such as by pharmacokinetic analysis. Suitable techniques will be clear to the person skilled in the art, and may, for example, generally involve the steps of suitably administering to a subject a suitable dose of the amino acid sequence or compound of the invention; collecting blood samples or other samples from the subject at regular intervals; determining the level or concentration of the amino acid sequence or compound of the invention in said blood sample; and calculating, from (a plot of) the data thus obtained, the time until the level or concentration of the amino acid sequence or compound of the invention has been reduced by 50% compared to the initial level upon dosing. Reference is, for example, made to the standard handbooks, such as Kenneth, A. et al., Chemical Stability of Pharmaceuticals: A Handbook for Pharmacists and in Peters et al., Pharmacokinetic Analysis: A Practical Approach (1996). Reference is also made to Gibaldi, M. et al., Pharmacokinetics, Second Rev. Edition, Marcel Dekker (1982).

Half-life can be expressed using parameters such as the t_(1/2)-alpha, t_(1/2)-beta, HL_Lambda_z, and the area under the curve (AUC). In the present specification, an “increase in half-life” refers to an increase in any one of these parameters, any two of these parameters, any three of these parameters or all four of these parameters.

The notations “mpk”, “mg/kg”, or “mg per kg” refer to milligrams per kilogram. All notations are used interchangeably throughout the present disclosure.

The terms “individual”, “subject”, and “patient”, used interchangeably herein, refer to an animal, preferably a mammalian (including a nonprimate and a primate), including, but not limited to, murines, simians, humans, mammalian farm animals (e.g., bovine, porcine, ovine), mammalian sport animals (e.g., equine), and mammalian pets (e.g., canine and feline); preferably the term refers to humans. In a certain embodiment, the subject, is a mammal, is preferably a human and is infected with HIV.

The term “therapeutically effective amount” refers to at least the minimal dose, but less than a toxic dose, of an agent which is necessary to impart a therapeutic benefit to a subject. For example, a therapeutically effective amount of a Combinectin of the invention is an amount which in mammals, preferably humans, results in a significant decline in circulating HIV within the infected individual.

Overview

The present invention provides novel polypeptides that bind to CD4 and/or gp41. The polypeptides comprising a CD4 binding moiety, a gp41 binding moiety, a HIV fusion peptide inhibitor moiety and combinations thereof. More specifically, the present invention relates to polypeptides comprising a fibronectin-based scaffold domain protein that binds CD4, a fibronectin-based scaffold domain protein that binds the N17 domain of gp41, and a HIV fusion peptide inhibitor or combinations thereof (herein referred to as “Combinectins”).

In order to identify CD4 and gp41 Adnectins™, soluble CD4 (extracellular domain) and gp41 (various artificial constructs designed to display a triple-helical segment mimicking a portion of gp41) were presented to large synthetic libraries of Adnectins™. Adnectins™ that survived several rounds of selection were screened for CD4 or gp41 binding, for biophysical properties, and for HIV-1 inhibitory activity. The best anti-CD4 and anti-N17 Adnectin™ sequences that emerged from the screenings were mutated and subjected to further rounds of selection with increased selective pressure, achieved by lowering the target concentration and/or selecting for anti-CD4 or gp41 Adnectins™ with fast on-rates and/or slow off-rates. From this optimization process, multiple families of Adnectins™, some that targeted CD4, and others targeting gp41, were identified as HIV-1 specific inhibitors with favorable biochemical and biophysical activity.

An optimized gp41-targeting helical peptide was developed starting with sequences related to gp41 HR2 and containing changes for improving potency and breadth across HIV strains as well as increasing the resistance barrier. Peptides were produced at times synthetically and at other times as genetic fusions to inert or active Adnectins™. Optimal N- and C-terminal positions were determined in fusions to a member of the gp41 Adnectin™ family. To identify mutations that would further increase potency, an N-terminally trimmed peptide with modest potency was used, so that improvements would be more easily detected. Small libraries of the inert Adnectin™-peptide fusion were made comprising single and multiple point mutations, then the proteins were expressed and screened for biophysical properties and HIV-1 inhibitory activity. The final family of peptides consisted of optimal length peptides with various combinations of the sequences that had the most favorable profiles.

I. Fibronectin Based Scaffolds—Adnectins™

One aspect of the application provides anti-CD4 and anti-N17 Adnectins™comprising a fibronectin type III (Fn3) domain in which part or all of one or more of the solvent accessible loops has been randomized or mutated. In some embodiments, one or more residues in one or more of the non-loop beta strands has also been randomized or mutated. In some embodiments, the Fn3 domain is an Fn3 domain derived from the tenth type 3 module of human fibronectin (¹⁰Fn3):

VSDVPRDLEVVAATPTSLLISWDAPAVTVRYYRITYGETGGNSPVQEFTVPGS KSTATISGLKPGVDYTITVYAVTGRGDSPASSKPISINYRT (SEQ ID NO:1) (BC, CD, DE, and FG loops are underlined)

(BC, CD, DE, and FG loops are underlined) (SEQ ID NO: 1) VSDVPRDLEVVAATPTSLLISWDAPAVTVRYYRITYGETGGNSPVQE FTVPGSKSTATISGLKPGVDYTITVYAVTGRGDSPASSKPISINYRT

In other embodiments, the non-ligand binding sequences of ¹⁰Fn3, i.e., the “¹⁰Fn3 scaffold”, may be altered, provided that the ¹⁰Fn3 retains ligand binding function and/or structural stability. A variety of mutant ¹⁰Fn3 scaffolds have been reported. In one aspect, one or more of Asp 7, Glu 9, and Asp 23 is replaced by another amino acid, such as, for example, a non-negatively charged amino acid residue (e.g., Asn, Lys, etc.). These mutations have been reported to have the effect of promoting greater stability of the mutant ¹⁰Fn3 at neutral pH as compared to the wild-type form (see, e.g., PCT Publication No. WO 02/04523). A variety of additional alterations in the ¹⁰Fn3 scaffold that are either beneficial or neutral have been disclosed. See, for example, Baton et al., Protein Eng., 15(12):1015-1020 (December 2002); Koide et al., Biochemistry, 40(34):10326-10333 (Aug. 28, 2001).

Both variant and wild-type ¹⁰Fn3 proteins are characterized by the same structure, namely seven beta-strand domain sequences designated A through G and six loop regions (AB loop, BC loop, CD loop, DE loop, EF loop, and FG loop) which connect the seven beta-strand domain sequences. The beta strands positioned closest to the N- and C-termini may adopt a beta-like conformation in solution. In SEQ ID NO:1, the AB loop corresponds to residues 14-17, the BC loop corresponds to residues 23-31, the CD loop corresponds to residues 37-47, the DE loop corresponds to residues 51-56, the EF loop corresponds to residues 63-67, and the FG loop corresponds to residues 75-87.

Accordingly, in some embodiments, the anti-CD4 or anti-N17 Adnectin™ of the invention is a ¹⁰Fn3 polypeptide that is at least 40%, 50%, 60%, 65%, 70%, 75%, 80%, 85%, or 90% identical to the human ¹⁰Fn3 domain, shown in SEQ ID NO:1. Much of the variability will generally occur in one or more of the loops. Each of the beta or beta-like strands of a ¹⁰Fn3 polypeptide may consist essentially of an amino acid sequence that is at least 40%, 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% identical to the sequence of a corresponding beta or beta-like strand of SEQ ID NO:1, provided that such variation does not disrupt the stability of the polypeptide in physiological conditions.

In some embodiments, the invention provides one or more Adnectins™ comprising a tenth fibronectin type III (¹⁰Fn3) domain, wherein the ¹⁰Fn3 domain comprises a loop, AB; a loop, BC; a loop, CD; a loop, DE; a loop EF; and a loop FG; and has at least one loop selected from loop BC, CD, DE, and FG with an altered amino acid sequence relative to the sequence of the corresponding loop of the human ¹⁰Fn3 domain. In some embodiments, the Adnectins™ of the present invention comprise an ¹⁰Fn3 domain comprising an amino acid sequence at least 40%, 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the non-loop regions of SEQ ID NO:1, wherein at least one loop selected from BC, CD, DE, and FG is altered. In some embodiments, the BC and FG loops are altered, and in some embodiments, the BC, DE, and FG loops are altered, i.e., the ¹⁰Fn3 domains comprise non-naturally occurring loops. In some embodiments, the AB, CD and/or the EF loops are altered. In some embodiments the CD and FG loops are altered. In some embodiments the solvent-accessible amino acids in the strands between loops are altered, with or without alteration of the adjoining loops. By “altered” is meant one or more amino acid sequence alterations relative to a template sequence (corresponding human fibronectin domain) and includes amino acid additions, deletions, substitutions or a combination thereof. Altering an amino acid sequence may be accomplished through intentional, blind, or spontaneous sequence variation, generally of a nucleic acid coding sequence, and may occur by any technique, for example, PCR, error-prone PCR, or chemical DNA synthesis.

In some embodiments, one or more loops selected from BC, CD, DE, and FG may be extended or shortened in length relative to the corresponding human fibronectin loop. In some embodiments, the length of the loop may be extended by 1-25 amino acids. In some embodiments, the length of the loop may be decreased by 1-11 amino acids. To optimize antigen binding, therefore, a loop of ¹⁰Fn3 may be altered in length as well as in sequence to obtain the greatest possible flexibility and affinity in antigen binding.

In some embodiments, the Adnectins™ comprise a Fn3 domain that comprises an amino acid sequence at least 40%, 50%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99%, or 100% identical to the non-loop regions of SEQ ID NO:1, wherein at least one loop selected from BC, CD, DE, and FG is altered. In some embodiments, the altered BC loop has up to 1, 2, 3, 4, 5, 6, 7, 8 or 9 amino acid substitutions, up to 1, 2, 3, or 4 amino acid deletions, up to 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acid insertions, or a combination thereof. In some embodiments, the altered CD loop has up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11 amino acid substitutions, up to 1, 2, 3, 4, 5, or 6 amino acid deletions, up to 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acid insertions, or a combination thereof. In some embodiments, the altered DE loop has up to 1, 2, 3, 4, 5, or 6 amino acid substitutions, up to 1, 2, 3, or 4 amino acid deletions, up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13 amino acid insertions, or a combination thereof. In some embodiments, the FG loop has up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 or 13 amino acid substitutions, up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11 amino acid deletions, up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25 amino acid insertions, or a combination thereof.

Extension Sequences

In certain embodiments, the Adnectin™ molecules of the present invention may be modified to comprise an N-terminal extension sequence and/or a C-terminal extension. For example, an MG sequence may be placed at the N-terminus of the ¹⁰Fn3 defined by SEQ ID NO: 1. The M will usually be cleaved off, leaving a G at the N-terminus. The Adnectins™ described herein may also comprise alternative C-terminal tail sequences, referred to herein as truncated C-terminal or C-terminal extension sequences. Further, truncated version may be used as therapeutic molecules in the truncated form, or alternative C-terminal extensions, such as His6 tag, may be added to the truncated version. In certain embodiments, the C-terminal extension sequences (also called “tails”), comprise E and D residues, and may be between 8 and 50, 10 and 30, 10 and 20, 5 and 10, and 2 and 4 amino acids in length. In certain embodiments, the first residue of a C-terminal extension is a proline. In certain other embodiments, the first residue of a C-terminal extension is a glutamic acid.

In some embodiments, the N-terminus may be extended by up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or more amino acids, which may be altered in any way, before or after rounds of selection, in order to improve target binding, stability, or both. In other embodiments, the C-terminus may be extended by up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or more amino acids, which may be altered in any way, before or after rounds of selection, in order to improve target binding, stability, or both. In still other embodiments, both the N- and C-termini may be extended in this manner.

Anti-CD4 Adnectin™

The amino acid sequence of anti-CD4 Adnectin™ loop region CD and FG of the invention include but are not limited to those listed in Table 1 below. The CD loops described in Table 1 replace R30 through T49 of ¹⁰Fn3 defined by SEQ ID NO:1. The FG loops described in Table 1 replace D67 through N91 of ¹⁰Fn3 defined by SEQ ID NO:1.

Table 1 also lists the IC₅₀ values for each anti-CD4 Adnectin™ comprising the listed CD/FG loop combinations.

TABLE 1 CD4 Adnectin ™-CD and FG loop combinations CD loop FG loop IC₅₀, μM SEQ ID NO HSYHIQYWPLGSYQRY EYQIRVYAETGGADSDQSM 0.0025 13, 14 QVFS GWIQIG LSYHIQYWPLGLYQAY EYQIRVYAETGRGESPASFG 0.0060 15, 16 QVFS WIQIG HAYHIQYWPLGFYQGY EYQIRVYAETGLGDAHQSLG 0.0072 17, 18 QVFS WIQIG LAYHIQYWPLGWYQR EYQIRVYAETGRGESPASFG 0.0075 19, 20 YQIFS WIQIG LAYHIQYWPLGWYQR EYQIRVYAETGRGESPASFG 0.0082 21, 22 YQVFS WIQIG HFYHIQYWPLGLYHLY EYQIRVYAETGRGESPASFG 0.0087 23, 24 QVFS WIQIG YSYHIQYWPLGWYHR EYQIRVYAETGADDPVQAL 0.0099 25, 26 YQVFS GWIQIG RCYHIQYWPLGLYPLY EYQIRVYAETGDESSVQPFG 0.0115 27, 28 QVFS WIQIG YSYHIQYWPLGWYQR EYQIRVYAETDGGRSQQSFG 0.0118 29, 30 YQVFS WIQIG SSYHIQYWPLGAYQRY EYQIRVYAETGRGESPASFG 0.0158 31, 32 QVFS WIQIG HAYHIQYWPLGLYQRY EYQIRVYAETGRGESPASFG 0.0165 33, 34 QVFS WIQIG HAYYIQYWPLGSYQFY EYQIRVYAETGRGESPASFG 0.0213 35, 36 QVFA WIQIG HSYHIQYWPLGSYLRY EYQIRVYAETGRGESPASFG 0.0214 37, 38 QVFS WIQIG LSYHIQYWPLGFYQRY EYQIRVYAETGRGESPASFG 0.0230 39, 40 QVFS WIQIG SAYHIQYWPLGWYHR EYQIRVYAETGRGESPASFG 0.0239 41, 42 YQIFS WIQIG YSYHIQYWPLGAYSRH EYQIRVYAETGGDGSEMYF 0.0260 43, 44 QLFS GWIQIG LAYHIQYWPLGWYHL EYQIRVYAETGRGESPASFG 0.0272 45, 46 YQVFS WIQIG LAYHIQYWPLGWYQL DYQIRVYAETSGESSEQYLG 0.0287 47, 48 YKVFS WIQIG HSYHIQYWPLGWYQL EYQIRVYAETEVDSGQHSFG 0.0290 49, 50 YQVFS WIQIG LAYHIQYWPLGWYQR EYQIRVYAETGESGAQQSFG 0.0297 51, 52 YQIFS WIQIG QSYHIQYWPLGAYQLY EYQIRVYAETGRGESPASFG 0.0323 53, 54 QLFS WIQIG HAYHIQYWPLGFYQGY EYQIRVYADTGRGYQLSYS 0.0353 55, 56 QVFS WIQIGY FRYHIQYWPLGGYERY EYQIRVYAETGRGESPASFG 0.0410 57, 58 QVFT WIQIG HSYHIQYWPLGSYHLY EYQIRVYAETGRGESPASFG 0.0411 59, 60 QLFS WIQIG HSYHIQYWPLGWYQL EYQIRVYAETGGFGSPPNFG 0.0436 61, 62 YQVFT WIQIG QFYHIQYWPLGSYQRY EYQIRVYAETGRGESPASFG 0.0509 63, 64 QVFS WIQIG NSYHIQYWPLGWYHR EYQIRVYAETGRGESPASFG 0.0517 65, 66 YQVFS WIQIG HSYHIQYWPLGRYQLY EYQIRVYAETGRGESPASFG 0.0562 67, 68 QVFS WIQIG LAYHIQYWPLGWYHL EYQIRVYAETGGVGWHHSF 0.0587 69, 70 YQIFS GWIQIG HVYHIQYWPLGWYPR EYQIRVYAETGRGESPASFG 0.0604 71, 72 YQVFS WIQIG HSYHIPYWELAWYQRY EYQIRVYAETGRGESPASFG 0.0637 73, 74 QVFS WIQIG ESYHIQYWPLGLYHRY EYQIRVYAETGRGESPASFG 0.0688 75, 76 QVFS WIQIG LAYHIQYWPLGWYQA EYQIRVYAETGRGESPASFG 0.0703 77, 78 YQVFS WIQIG YLYHIQYWPLGWYHR EYQIRVYAETGRGESPASFG 0.0715 79, 80 YQVFT WIQIG RFYHIQYWPLGWYHC EYQIRVYAQTGDGSSQEYFG 0.0839 81, 82 YQVFV WIQIG HSYHIQYWPLGWYYR EYQIRVYAETGGSGSQQYVV 0.0869 83, 84 YQVFS GWIQIG HAYHIQYWPLGFYQGY EYQIRVYAETGRGESPASFG 0.0875 85, 86 QVFS WIQIG HSYHIQYWPLGLYVLY EYQIRVYAETGAGGSEHSFG 0.1059 87, 88 QVFS WIQIG LSYHIQYWPLGRYERY EYQIRVYAETVGGESLDSFS 0.1277 89, 90 QVFS WIQIG LSYHIQYWPLGWYQLY EYQIRVYAETRVGGSVASFG 0.1600 91, 92 QVFY WIQIG LAYHIQYWPLGRYQLY EYQIRVYAETGRGESPASFG 0.4281 93, 94 QVFS WIQIG

In some embodiments, anti-CD4 Adnectin™ of the invention comprises an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the CD/FG loop region combinations of SEQ ID NOs: 13-94.

In some embodiments, anti-CD4 Adnectin™ of the invention comprises an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of the CD loop regions of SEQ ID NOs: 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37, 39, 41, 43, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73, 75, 77, 79, 81, 83, 85, 87, 89, 91 and 93.

In some embodiments, anti-CD4 Adnectin™ of the invention comprises an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of the FG loop regions of SEQ ID NOs: 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92 and 94.

WebLogo (≤weblogo.berkeley.edu≥) was used to identify consensus sequences for anti-CD4 Adnectin™. Y32, I34, Y36, Q46 and F48 of the anti-CD4 Adnectin™ CD loop are conserved amino acids (see FIG. 6). In some embodiments, the anti-CD4 Adnectin™ comprises one or more of the conserved amino acids Y32, I34, Y36, Q46 and F48.

WebLogo identified Y68, I70, V72, A74, T76, I88 and I90 of the anti-CD4 Adnectin™ FG loop as conserved amino acids (see FIG. 7). In some embodiments, the anti-CD4 Adnectin™ comprises one or more of the conserved amino acids Y68, I70, V72, A74, T76, I88 and 190.

In some embodiments, the anti-CD4 Adnectin™ comprises one or more of the conserved amino acids Y32, I34, Y36, Q46, F48, Y68, I70, V72, A74, T76, I88 and 190.

The full length amino acid sequence of anti-CD4 Adnectin™ of the invention include but are not limited to those listed in Table 2 below. Table 2 also lists the antiviral EC₅₀ values for each anti-CD4 Adnectin™

TABLE 2 Anti-CD4 Adnectin ™ SEQ ID Antiviral NO EC₅₀ (nM) Anti-CD4 Adnectin ™ Protein Sequence  95    48 MASTSGVSDVPRDLEVVAATPTSLLISWDAPAVTVHS YHIQYWPLGWYQRYQVFSVPGSKSTATISGLKPEVEY QIRVYAETGGGGSQQSFGWIQIGYRTEGSGSHHHHHH  96     7.8 MGVSDVPRDLEVVAATPTSLLISWDAPAVTVQSYHIQ YWPLGSYQRYQVFSVPGSKSTATISGLKPGVEYQIRV YAETGGADSDQSMGWIQIGYRTEGDKPSQHHHHHH  97    11 MGVSDVPRDLEVVAATPTSLLISWDAPAVTVHSYHIQ YWPLGWYQRYQVFSVPGSKSTATISGLKPGVEYQIRV YAETRSGLADESFGWIQIGYRTEGDKPSQHHHHHH  98     4.9 MGVSDVPRDLEVVAATPTSLLISWDAPAVTVHSYHIQ YWPLGSYQRYQVFSVPGSKSTATISGLKPGVEYQIRV YAETGGADSDQSMGWIQIGYRTEGDKPSQHHHHHH  99     8.5 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWDAPA VTVHSYHIQYWPLGSYQRYQVFSVPGSKSTATISGLK PGVEYQIRVYAETGGADSDQSFGWIQIGYRTPES 100     6 MASTSGSSSYLMPSDLEVVAATPTSLYIHWYPIASTIIN FRITYGETGGNSPVQEFTVPGSQVHATISGLKPGVDYT ITVYAVHYEHKYSELWMGHPISINYRTEGSGSHHHHH H 101  >400 MASTSGSASYLIPSDLEVVAATPTSLSIYWYPVASTIIN FRITYVETGGNSPVQEFTVPGSKSTATISGLKPGVDYTI TVYAVHYEQKYSEYWIGHPISINYRTEGSGSHHHHHH 102 >5500 MASTSGSSPYLMPYDLEVVAATPTSLFIRWYGSASSIV KFRITYGETGGNSPVQEFTVGGTQLHATISGLKPGVD YTITVYAVHFEHKYSELWIGHPISINYRTEGSGSHHHH RH 103   255 MASTSGYTSYPIPYDLEVVAATPTSLYIHWYWIAATII SFRITYGETGGNSPVQEFTVPAGQDHATISGLKPGVDY TITVYAVHYEEEYSEFWTGHPISINYRTEGSGSHHHHH H 104   500 MASTSGTHWFYSIPHDLEVVAATPTSLTIAWEPPHHT AMGYRITYGETGGNSPVQEFTVPGGYTTAYISGLKPG VDYTITVYAAYYEREYSEHWISHPISINYRTEGSGSHH HHHH 105   300 MASTSGEFYHTKYPYDLEVVAATPTSLEISWRSPTRD WQWFRITYGETGGNSPVQEFTVAGPYRNAIISGLKPG VDYTITVYADVYMPSEGGLVVDTYHPISINYRTEGSG SHHHHHH 106  2400 MASTSGQAYPEYYFVDLEVVAATPTSLLISWSKPYYN AYSYRITYGETGGNSPVQEFTVLGHDTRAVISGLKPG VDYTITVYAMFIEYIDQEIWHAHPISINYRTEGSGSHH HHHH 107   500 MGVSDVPRDLEVVAATPTSLLISWDEHTDIYRYYRIT YGETGGNSPVQEFTVPAMEHTATISGLKPGVDYTITV YAVTHVYPIMIHQYPISINYRTEIDKPSQHHHHHH 108   170 MASTSGVSDVPRDLEVVAATPTSLLISWDAPAVTVLE YQIDYHPAAVWHALQRFTVPGSKSTATISGLKPGVHY KISVTATTHADNESIMWHPISIYYRTEGSGSHHHHHH 109   320 MGVSDVPRDLEVVAATPTSLLISWDYPTVTPRYYRIT YGETGGNSPVQEFTVPEYIGTATISGLKPGVDYTITVY AVTNDTTIYSISRPISINYRTEIDKPSQHHHHHH 110    28.6 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWDAPA VTVHSYHIQYWPLGSYQRYQVFSVPGSKSTATISGLK PGVEYQIRVYAETGRGESDQSLGWIQIGYRTEES 111    20.0 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWDAPA VTVHSYHIQYWPLGSYQRYQVFSVPGSKSTATISGLK PGVEYQIRVYAETGRGESDQSFGWIQIGYRTEES 112    18.4 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWDAPA VTVHSYHIQYWPLGSYQRYQVFSVPGSKSTATISGLK PGVEYQIRVYAETGRGESDQSLGWIQIGYRTPES 113    15.4 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWDAPA VTVHSYHIQYWPLGSYQRYQVFSVPGSKSTATISGLK PGVEYQIRVYAETGRGESDQSFGWIQIGYRTPES 114    12.6 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWDAPA VTVHAYHIQYWPLGFYQGYQVFSVPGSKSTATISGLK PGVEYQIRVYAETGLGDAHQSLGWIQIGYRTPES

In some embodiments, the anti-CD4 Adnectin™ of the invention comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 95-114.

In some embodiments, the anti-CD4 Adnectin™ of the invention comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 95-114, excluding any N-terminus extended region.

In some embodiments, the anti-CD4 Adnectin™ of the invention comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 95-114, excluding any C-terminus extended region.

In some embodiments, the anti-CD4 Adnectin™ of the invention comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 95-114, excluding both the N-terminus and C-terminus extended regions.

In other embodiments, anti-CD4 Adnectin™ comprises an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the CD loop and FG loop regions of SEQ ID NOs: 95-114.

Anti-N17 Adnectin™

The full length amino acid sequence of anti-N17 Adnectin™ protein of the invention include but are not limited to those listed in Table 3 below. Table 3 also lists the antiviral EC₅₀ values for each anti-N17 Adnectin™.

TABLE 3 Anti-N17 Adnectin ™ SEQ ID Antiviral NO EC₅₀ (nM) Anti-N17 Adnectin ™ Protein Sequence 115 130 MGVSDVPRDLEVVAATPTSLLISWEYKVNNYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVHSSPISINYRTEIDKPSQHHHHHH 116 50 MASTSGVSDVPRDLEVVAATPTSLLISWDAPAVTVEQY YIAYYVEGEPSSYQYFRVPGSKSTATISGLKPGVLYHIY VNAVTGSGLRPEFSLPIRIKYRTEGSGSHHHHHH 117 42 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 118 28 MGVSDVPRDLEVVAATPTSLLISWKYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVNSLPISINYRTEIDKPSQHHHHHH 119 >1,000 MGVSDVPRDLEVVAATPTSLLISWDAPAVTVGWYHIGY NVEGEPASYQYFRVPGSKSTATISGLKPGVEYMIFVNAV TGSGAREEFSLPISINYRTEGSGSHHHHHH 120 39 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWEYNVN PYRYYRITYGETGGNSPVQEFTVPSVLSSAQISGLKPGV DYTITVYAVTRGVDSAPISINYRTPGG 121 57 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWEYNVN PYRYYRITYGETGGNSPVQEFTVPSVLSTAEISGLKPGV DYTITVYAVTYGVDSDPISINYRTPGG 122 6 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWQYKVH PYRYYRITYGETGGNSPVQEFTVPSVLSTAEISGLKPGV DYTITVYAVTRGVDSAPISINYRTPGG 123 28 MGVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TRGVDSAPISINYRTEIDKPSQHHHHHH 124 6 MGVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTAEISGLKPGVDYTITVYAV TRGVDSAPISINYRTPIDKPSQHHHHHH 125 4342 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWEYKVH PYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGVQSDPISINYRTPGG 126 8 MGVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGIQSPPISINYRTEIDKPSQHHHHHH 127 9 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWQYKVH PYRYYRITYGETGGNSPVQEFTVPSVLSSAQISGLKPGV DYTITVYAVTYGIESSPISINYRTPGG 128 18 MGHHHHHHGGVSDVPRDLEVVAATPTSLLISWEYKVH PYRYYRITYGETGGNSPVQEFTVPSVLSSAEISGLKPGVD YTITVYAVTYGIDSSPISINYRTPGG 129 11 MGVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSSAEISGLKPGVDYTITVYAV TYGIDSPPISINYRTEIDKPSQHHHHHH 130 42 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYNV HYDRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTDGVHSSPISINYRTEID 131 5 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDLSAPISINYRTEID 132 5 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWDAPA VTVEEYYIGYYVEFEPSSYQWFTVPGSKSTATISGLKPG VEYSIYVNAVTGMGMQPEMSLPISINYRTEGS 133 42 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HYDRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGVDSDPISINYRTEID 134 5 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWDAPA VTVEQYYIAYYDEKEPSSYQYFRVPGSKSTATISGLKPG VEYAIFVNAVTRSGVLPEFSLPISINYRTEGS 135 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWKYNV NAYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGVHSSPISINYRTEID 136 5 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWDAPA VVTVEQYYIGYYVEAEPSSYQYFFVPGSKSTATISGLKPG VDYAIFVNAVTASGRGPEYSLPISINYRTEGS 137 80 MGVSDVPRDLEVVAATPTSLLISWHDGIGEERYYRITYG ETGGNSPVQEFTVPMDDITATISGLKPGVDYTITVYAVT VGDVISVLHEPISINYRTEIDKPSQHHHHHH 138 3300 MGVSDVPRDLEVVAATPTSLLISWHYPFEGYVTYYRIT YGETGGNSHVQEFTVPVGYTTATISGLKPGVDYTITVYA VTSSKGYVYFPISINYRTEIDKPSQHHHHHH 139 130 MGVSDVPRDLEVVAATPTSLLISWEDPEAAVRYYRITY GETGGNSPVQEFTVPINDLHSYLSGLKPGVDYTITVYAV TEATVMYVLDEPISINYRTEIDKPSQHHHHHH 140 950 MGVSDVPRDLEVVAATPTSLLISWDLLEDMSRYYRITY GETGGNSPVQEFTVPTDAYTATISGLKPGVDYTITVYAV TQDSHVIELSYPISINYRTEIDKPSQHHHHHH 141 3 MGVSDVPRDLEVVAATPTSLLISWQYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGIQSPPISINYRTEIDKPSQHHHHHH 142 55 MGVSDVPRDLEVVAATPTSLLISWRYRVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TDGVQSSPISINYRTEIDKPSQHHHHHH 143 20 MGVSDVPRDLEVVAATPTSLLISWEYNVNPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGIESSPISINYRTEIDKPSQHHHHHH 144 20 MGVSDVPRDLEVVAATPTSLLISWQYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVESSPISINYRTEIDKPSQHHHHHH 145 11 MGVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVNSLPISINYRTEIDKPSQHHHHHH 146 11 MGVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGIDSPPISINYRTEIDKPSQHHHHHH 147 28 MGVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVDSDPISINYRTEIDKPSQHHHHHH 148 14 MGVSDVPRDLEVVAATPTSLLISWEYNVNPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGIDSPPISINYRTEIDKPSQHHHHHH 149 3 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGKDSAPISINYRTEID 150 18 MGVSDVPRDLEVVAATPTSLLISWEYNVNPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVESSPISINYRTEIDKPSQHHHHHH 151 11 MGVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGIDSSPISINYRTEIDKPSQHHHHHH 152 20 MGVSDVPRDLEVVAATPTSLLISWEYNVNPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVQSDPISINYRTEIDKPSQHHHHHH 153 8 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTAQISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 154 8 MGVSDVPRDLEVVAATPTSLLISWEYNVNPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVNSLPISINYRTEIDKPSQHHHHHH 155 9 MGVSDVPRDLEVVAATPTSLLISWQYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV THGVHSAPISINYRTEIDKPSQHHHHHH 156 43 MGVSDVPRDLEVVAATPTSLLISWEYKVNPWRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGIESSPISINYRTEIDKPSQHHHHHH 157 43 MGVSDVPRDLEVVAATPTSLLISWQYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVNSIPISINYRTEIDKPSQHHHHHH 158 85 MGVSDVPRDLEVVAATPTSLLISWEYKVHYDRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGIQSPPISINYRTEIDKPSQHHHHHH 159 23 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISIPYRTPGG 160 58 MGVSDVPRDLEVVAATPTSLLISWEYKVDPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVESSPISINYRTEIDKPSQHHHHHH 161 13 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSSAEISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 162 35 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSSAQISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 163 35 MGHHHHHHGGSVSDVPRYLEVVAATPTSLLISWQYKV HPYRWYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGVNSIPISINYRTEID 164 35 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWKYQV HAYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGVYSAPISINYRTEID 165 42 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV NPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGVHSSPISINYRTEID 166 50 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWKYNL HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGIISEPISINYRTEID 167 42 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYRV NPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGVQSPPISINYRTEID 168 42 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV NAYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGVLSPPISINYRTEID 169 5 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYNV NPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTRGVDSAPISINYRTEID 170 5 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVS PYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTFGIRSSPISINYRTEID 171 35 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWKYQV HAYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGIISEPISINYRTEID 172 5 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGIDSSPISINYRTEID 173 5 MGHHHHHHGGAVSDVPRDLEVVAATPTSLLISWEYKV NPWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGVHSSPISINYRTEID 174 5 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYNV NAYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGIISEPISINYRTEID 175 5 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HYDRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGVQSTPISINYRTEID 176 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HHDRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGIESSPISINYRTEID 177 252 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISIPYRTPGG 178 631 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGXDSXPISINYRTEID 179 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSRPISINYRTEID 180 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGKDSAPISINYRTEID 181 631 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDHSAPISINYRTEID 182 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDQSAPISINYRTEID 183 20 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGIDSAPISINYRTEID 184 20 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDVSAPISINYRTEID 185 252 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGXDSAPISINYRTEID 186 2830 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGEDSAPISINYRTEID 187 86 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFKVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 188 86 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDLSAPISINYRTEID 189 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGKDSAPISINYRTEID 190 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGADSAPISINYRTEID 191 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGTDSAPISINYRTEID 192 2830 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGTDSAPISINYRTEID 193 252 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGKDSAPISINYRTEID 194 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDPSAPISINYRTEID 195 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSQPISINYRTEID 196 86 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDVSAPISINYRTEID 197 81 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSGPISINYRTEID 198 2830 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISIQYRTEID 199 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSQPISINYRTEID 200 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYTETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 201 20 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDQSAPISINYRTEID 202 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSKPISINYRTEID 203 86 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSGPISINYRTEID 204 0 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYRETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 205 86 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYDV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 206 237 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSKPISINYRTEID 207 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYWETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 208 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSTPISINYRTEID 209 20 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSTPISINYRTEID 210 143 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSSPISINYRTEID 211 631 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTRGDDSAPISINYRTEID 212 86 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTHGDDSAPISINYRTEID 213 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSWPISINYRTEID 214 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTHGDDSAPISINYRTEID 215 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWKYDV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 216 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISDLKPG VDYTITVYAVTYGDDSHPISINYRTEID 217 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTRGDDSAPISINYRTEID 218 62 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATIRGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 219 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWKYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 220 86 MGHHHHHHCGSVSDVPRDLEVVAATPTSLLISWEYKV AHNRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 221 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV YGYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 222 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DHQRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 223 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DYRRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 224 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV AYDRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 225 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV TSYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 226 631 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRIIHETGGNSPVQEFTVPSVLSTATISGLKPGVD YTITVYAVTYGDDSAPISINYRTEID 227 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRKEAEL 228 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV NHQRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 229 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DHRRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 230 17 MGVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVDSDPISINYRTDDKPSQHHHHHH 231 10 MGVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVNSIPISINYRTEIDKPSQHHHHHH 232 47 MGVSDVPRDLEVVAATPTSLLISWEYKVNAYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGIESSPISINYRTEIDKPSQHHHHHH 233 55 MGVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TDGVQSSPISINYRTEIDKPSQHHHHHH 234 20 MGVSDVPRDLEVVAATPTSLLISWEYKVNAYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGIDSSPISINYRTEIDKPSQHHHHHH 235 29 MGVSDVPRDLEVVAATPTSLLISWEYKVHYDRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TNGVLSSPISINYRTEIDKPSQHHHHHH 236 85 MGVSDVPRDLEVVAATPTSLLISWEYKVNPWRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TRGVDSAPISINYRTEIDKPSQHHHHHH 237 31 MGVSDVPRDLEVVAATPTSLLISWEYKVHPXRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVBSXPISINYRTEIDKPSQHHHHHH 238 11 MGVSDVPRDLEVVAATPTSLLISWEYKVNPWRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGIQSPPISINYRTEIDKPSQHHHHHH 239 4 MGVSDVPRDLEVVAATPTSLLISWQYKVHPYRWYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVNSIPISINYRTEIDKPSQHHHHHH 240 5 MGVSDVPRDLEVVAATPTSLLISWEYKVSPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVNSIPISINYRTEIDKPSQHHHHHH 241 8 MGVSDVPRDLEVVAATPTSLLISWEYKVNPWRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVNSLPISINYRTEIDKPSQHHHHHH 242 0 MGVSDVPRDLEVVAATPTSLLISWEYNVHYDRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVDSDPISINYRTEIDKPSQHHHHHH 243 48 MGVSDVPRDLEVVAATPTSLLISWEYKVNPWRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVDSDPISINYRTEIDKPSQHHHHHH 244 58 MGVSDVPRDLEVVAATPTSLLISWEYKVDPYRYYRITY GETGGNSPVQEFTVPSVLSTATISGLKPGVDYTITVYAV TYGVDSDPISINYRTEIDKPSQHHHHHH 245 50 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWKYQV HAYRYYRITYGETGGNSPVQEFTVPSVLSTATINGLKPG VDYTITVYAVTYGIISEPISINYRTEID 246 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV NYNRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTEGVQSAPISINYRTEID 247 2 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTPGG 248 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNTPVQEFRVPSVLSTATISGLKPG VDYTITVYAVTYADASAPISINYRTEID 249 83 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSSATLNGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 250 218 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSSAKISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 251 186 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFNVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 252 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV AHRRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 253 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DAYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 254 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DSYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 255 136 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 256 170 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDASAPISINYRTEID 257 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTNGDDSAPISINYRTEID 258 195 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSSATIRGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 259 135 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTAKISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 260 188 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFRVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 261 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV APWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 262 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DGWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 263 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DTWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 264 209 MGHHHHHHGGSVSDVPRDLEVVAATPTXLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 265 63 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGADSAPISINYRTEID 266 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTRGDDSAPISINYRTEID 267 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQDFTVPSVLSTATIRGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 268 2 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTANISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 269 184 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQAFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 270 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV APYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 271 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DGYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 272 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DTYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 273 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYEV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 274 115 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYRV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 275 180 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQSFTVPSVLSTATISGLKPGV DYTITVYAVTYGADSAPISINYRTEID 276 16 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATIRGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 277 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQDFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 278 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV ARWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 279 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DHQRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 280 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DYGRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 281 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWKYGV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 282 56 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYSVH PYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 283 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTDGDDSAPISINYRTEID 284 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTSGDDSAPISINYRTEID 285 397 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSSATLRGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 286 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV AAWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 287 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV ATWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 288 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATTTSLLISWEYKV DYHRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 289 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYGV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 290 138 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWKYXV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 291 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTGGDDSAPISINYRTEID 292 52 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATIHGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 293 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATLRGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 294 101 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSSATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 295 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV AAYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 296 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV ATYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 297 30 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DPWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 298 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DYQRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 299 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWKYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 300 132 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYXV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 301 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTHGDDFAPISINYRTEMLI 302 4 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSSATINGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 303 109 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFKVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 304 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV AHDRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 305 83 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 306 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DYRRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 307 205 MGHHHHHHGGSVSDVPRDLEVVAATPTGLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 308 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV NAWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 309 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTHGDDSAPISINYRTEID 310 62 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATINGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 311 42 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTAEISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 312 37 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFLVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 313 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV AHGRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 314 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV AYKRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 315 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV DRWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 316 331 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYAV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 317 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV NAYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 318 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV NGYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 319 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVS HGRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 320 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV TTWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 321 55 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSSAZLSGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 322 96 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGTDSAPISINYRTEID 323 126 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDQSAPISINYRTEID 324 487 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSNPISINYRTEID 325 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV NHDRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 326 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVS HRRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 327 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV TYERYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 328 63 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSSATXXGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 329 102 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDVSAPISINYRTEID 330 99 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSPPISINYRTEID 331 100 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSXPISINYRTEID 332 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV NRWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 333 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVS PWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 334 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV TYRRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 335 112 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDESAPISINYRTEID 336 171 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSDPISINYRTEID 337 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSYPISINYRTEID 338 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV NRYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 339 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVS RWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 340 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV XXYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 341 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQSFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 342 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGIDSAPISINYRTEID 343 122 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDHSAPISINYRTEID 344 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSEPISINYRTEID 345 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSRPISINYRTEID 346 83 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISIQYRTEID 347 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV NYRRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 348 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVS TWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 349 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV YAYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 350 191 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQTFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 351 215 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQAFTVPSVLSTATISGLKPG VDYTITVYAVTYGKDSAPISINYRTEID 352 77 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDLSAPISINYRTEID 353 19 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSGPISINYRTEID 354 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVS AWRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 355 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVS TYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 356 31 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTAELSGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 357 178 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDLSAPISINYRTEID 358 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSTPISINYRTEID 359 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVS AYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 360 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV TGYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 361 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV YHGRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 362 121 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTAKLSGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 363 130 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGNDSAPISINYRTEID 364 89 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDPSAPISINYRTEID 365 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVS GYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGV DYTITVYAVTYGDDSAPISINYRTEID 366 >1,000 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV YHNRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 367 300 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSSAQLSGLKPG VDYTITVYAVTYGDDSAPISINYRTEID 368 62 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGTDSAPISINYRTEID 369 155 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDPSAPISINYRTEID 370 335 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGDDSKPISINYRTEID 371 114 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKV HPYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPG VDYTITVYAVTYGIDSTPISINYRTEID

In some embodiments, the anti-N17 Adnectin™ of the invention comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 115-371.

In some embodiments, the anti-N17 Adnectin™ of the invention comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 115-371, excluding any N-terminus extended region.

In some embodiments, the anti-N17 Adnectin™ of the invention comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 115-371, excluding any C-terminus extended region.

In some embodiments, the anti-N17 Adnectin™ of the invention comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 115-371, excluding both the N-terminus and C-terminus extended regions.

In other embodiments, anti-N17 Adnectin™ comprises an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the BC loop, DE loop and FG loop regions of SEQ ID NOs: 115-371.

Analysis of the sequences above indicate that S52, V53, L54 and S55 of the anti-N17 Adnectin™ DE loop are conserved amino acids. In some embodiments, the anti-N17 Adnectin™ comprises one or more of the conserved amino acids S52, V53, L54 and S55.

Additionally, analysis of the sequences above indicate that Y24 of the anti N17 Adnectin™ BC loop is a conserved amino acid. In some embodiments, position 26 of the anti-N17 Adnectin™ BC loop is valine or leucine.

Analysis of the sequences above indicate that G78 and S85 of the anti-N17 Adnectin™ FG loop are conserved amino acids. In some embodiments, the anti-N17 Adnectin™ comprises one or more of the conserved amino acids G78 and S85. In some embodiments, position 79 of the anti-N17 Adnectin™ FG loop is valine or isoleucine.

In some embodiments, the anti-N17 Adnectin™ comprises one or more of the conserved amino acids Y24, V26, L26, S52, V53, L54, S55 G78, V79, 179 and S85.

Point mutation analysis of the anti-N17 Adnectin™ showed advantages of mutating several ¹⁰Fn3 non-loop scaffold positions. Specifically, mutating positions T56 and T58 boosted potency. In some embodiments, the anti-N17 Adnectin™ comprises mutating T58 to Asn, Glu, or Gln.

II. HIV Fusion Peptide Inhibitors

The amino acid sequence of gp41, and its variation among different strains of HIV-1, is well known. The fusogenic domain (often called the fusion peptide, or FP) is believed to be involved in insertion into and disruption of the target cell membrane. The transmembrane domain, containing the transmembrane anchor sequence, is located toward the C-terminal end of the protein. Between the fusogenic domain and transmembrane anchor are two distinct regions, known as heptad repeat (HR) regions, each region having a plurality of heptads. The amino acid sequence comprising the HR1 region and the amino acid sequence comprising the HR2 region are each relatively conserved regions in the HIV-1 envelope protein. A representative sequence of the external domain of gp41 (clade B consensus) is as follows:

(SEQ ID NO: 2) 512 AVGIGAMFL GFLGAAGSTM GAASVTLTVQ ARQLLSGIVQ QQNNLLRAIE 561 AQQHLLQLTV WGIKQLQARV LAVERYLKDQ QLLGIWGCSG KLICTTAVPW 611 NASWSNKSLD EIWNNMTWME WEREIDNYTG LIYTLIEESQ NQQEKNEQEL 661 LELDKWASLW NWFDITNWLW YIK

The fusion peptide consists of approximately the first 23 amino acids, Ala512-Ser534. The HR1 region has a plurality of contiguous 7 amino acid residue stretches or “heptads” (the 7 amino acids in each heptad designated “a” through “g”), with a predominance of hydrophobic residues at the first (“a”) and fourth (“d”) positions which interact homotypically to form the core of the 3-helix bundle structure. Neutral polar amino acids such as Glutamine may also occupy these positions. One representative heptad begins with Leu545. A highly conserved portion of HR1 consists of the 17 residues from Leu565 to Leu581, and is called “N17”.

The C-terminal portion of gp41 comprises the HR2 region, which is believed to form an alpha helical structure during the fusion process, and bind into the grooves of the HR1 triple helical structure. HR2 also comprises heptads, though they do not interact homotypically but rather interact with amino acids from HR1. One representative heptad begins at Trp628.

HIV Fusion Peptide Inhibitor

The HIV fusion peptide inhibitor of the invention include but are not limited to the following sequences:

SEQ ID HIV Fusion Peptide Inhibitor Sequence NO SEYEARIEALIRAAQEQQEKNEAALRELYKWAL 372 SEYEARIEALIRAAQEQQEKNEAALRELWKWAS 373 TIAEYAARIEALIRAAQEQQEKNEAALRELYKWAS 374 ARIEEYAARIEALIRAAQEQQEKNEAALRELYKWAS 375 SEYEARIEALIRAAQEQQEKNEAALRELYKWAS 376 TEYEARIEALIRAAQEQQEKNEAALRELKEWASIWN 377 SEYEARIEALIRAAQEQQEKNEAALRELDKWTGVWGNYEKV 378 SRIEALIRAAQEQQEKNEAALRELFKWAS 379 SRIEALIRAAQEQQQKNEAALRELDKWAS 380 SRIEALIRAAQEQQEKNEAALRELYKWAS 381 SRIEALIRAAQEQQEKNEAALRELLKWAS 382 SRIEALIRAAQEQQEKNEAALRELQKWAS 383 SRIEALIRAAQEQQEKNEAALRELDKWAS 384 AIAEYAARIEALIRAAQEQQEKNEAALRELDKWAS 385 TEYEARIEALIRAAQEQQEKNEAALRELDK 386 SRIEALIRAAQEQQEKNEAALRELYKWTS 387 SRIEALIRAAQEQQEKNEAALRELYKWASLWI 388 SRIEALIRAAQEQQEKNEAALRELYKWASRWN 389 SRIEALIRAAQEQQEKNEAALRELYKWASSWN 390 SRIEALIRAAQEQQEKNEAALRELYKWGS 391 SRIEALIRAAQEQQEKNEAALRELDK 392

In some embodiments, the HIV fusion peptide inhibitor comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 372-392.

Point mutations in the C-terminal region of the HIV fusion peptide inhibitor were seen to boost potency. In some embodiments, a hydrophobic replacement of the aspartic acid (D) near the C-terminus of the HIV fusion peptide inhibitor provided at least a 10× increase in potency (FIG. 8). In some embodiments, the HIV fusion peptide inhibitor comprises replacing “DK” with “YK”, “LK”, “FK” or “WK”.

Other point mutation studies in the C-terminal region showed how the C-terminal amino acids “WAS” can be mutated with good effects on potency. In some embodiments, the HIV fusion peptide inhibitor comprises replacing C-terminal amino acids “WAS” to “WFS” or “WAL”.

III. Linkers

The various components of the Combinectin of the invention may be covalently or non-covalently linked. In some embodiments, the PK moiety may be directly or indirectly linked to a Combinectin via a polypeptide linker.

Suitable linkers are those which allow the separate domains to fold independently of each other forming a three dimensional structure that permits high affinity binding to a target molecule.

The disclosure provides a number of suitable linkers that meet these requirements, including glycine-serine based linkers, glycine-proline based linkers. The Examples described herein demonstrate that the Combinectin domains joined via polypeptide linkers retain their target binding function. In some embodiments, the linker is a glycine-serine based linker. These linkers comprise glycine and serine residues and may be between 8 and 50, 10 and 30, and 10 and 20 amino acids in length. Examples include linkers having an amino acid sequence (GS)₇ (SEQ ID NO: 393), G(GS)₆ (SEQ ID NO: 394), and G(GS)₇G (SEQ ID NO: 395). Other linkers contain glutamic acid, and include, for example, (GSE)₅ (SEQ ID NO: 396) and GGSEGGSE (SEQ ID NO: 397). Other exemplary glycine-serine linkers include (GS)₄ (SEQ ID NO: 398), (GGGGS)₇ (SEQ ID NO: 399), (GGGGS)₅ (SEQ ID NO: 400), (GGGGS)₄ (SEQ ID NO: 401 (GGGGS)₃G (SEQ ID NO: 402). In some embodiments, the linker is a glycine-proline based linker. These linkers comprise glycine and proline residues and may be between 3 and 30, 10 and 30, and 3 and 20 amino acids in length. Examples include linkers having an amino acid sequence (GP)₃G (SEQ ID NO: 403) and (GP)₅G (SEQ ID NO: 404). In other embodiments, the linker may be a proline-alanine based linker having between 3 and 30, 10 and 30, and 3 and 20 amino acids in length. Examples of proline alanine based linkers include, for example, (PA)₃ (SEQ ID NO: 405), (PA)₆ (SEQ ID NO: 406) and (PA)₉ (SEQ ID NO: 407). In some embodiments, the linker is a glutamic acid-proline based linker. These linkers comprise glutamic acid and proline residues and may be between 3 and 30, 10 and 30, and 3 and 20 amino acids in length. Examples include linkers having an amino acid sequence ESPEPETPEDE (SEQ ID NO: 408) and (ESPEPETPED)₂E (SEQ ID NO: 409). It is contemplated, that the optimal linker length and amino acid composition may be determined by routine experimentation by methods well known in the art.

Linkers or spacers, may be introduced at the N-terminus of the anti-CD4 moiety, the C-terminus of the anti-CD4 moiety, the N-terminus of the anti-gp41 moiety, the C-terminus of the anti-gp41 moiety, the N-terminus of the HIV fusion peptide inhibitor, or combinations thereof. In some embodiments the preferred linkers between the anti-CD4 Adnectin™ and anti-N17 Adnectin™ are short glutamine-proline rich linkers. In some embodiments the preferred linker between the anti-N17 Adnectin™ and HIV fusion peptide inhibitor are flexible glycine-serine rich linkers.

IV. Anti-N17 Adnectin™ Linked to a HIV Fusion Peptide Inhibitor Combinectin

The amino acid sequences of anti-N17 Adnectin™-HIV fusion peptide inhibitor Combinectin of the invention include but are not limited to those listed in Table 4 below. Table 4 also lists the antiviral EC₅₀ values for each anti-N17 Adnectin™-HIV fusion peptide inhibitor Combinectin.

TABLE 4 Anti-N17 Adnectin TM - HIV Fusion Peptide Inhibitor Combinectin SEQ Anti- ID viral Anti-N17 Adnectin ™ - HIV Fusion NO EC₅₀ (nM) Peptide Inhibitor Protein Sequence 410 2 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVN AYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGVD YTITVYAVTYGVDSDPISINYRTEIDGGGGSGGGGSGGG GSGGGGARIEEYAARIEALIRAAQEQQEKNEAALRELYK WAS 411 4342 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVN AYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGVD YTITVYAVTYGVDSDPISINYRTEIDGGGGSGGGGSGGG GSGGGGTIAEYAARIEALIRAAQEQQEKNEAALRELYK WAS 412 2980 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVN AYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGVD YTITVYAVTYGVDSDPISINYRTEIDGGGGSGGGGSGGG GSGGGGSEYEARIEALIRAAQEQQEKNEAALRELYKWAS 413 6 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWKYKVHP YRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGVDY TITVYAVTYGVNSLPISINYRTEIDGGGGSGGGGSGGGGS GGGGTEYEARIEALIRAAQEQQEKNEAALRELKEWASI WN 414 4 MGHHHHHHTSGVSDVPRDLEVVAATPTSLLISWDAPAV TVGWYHIGYNVEGEPASYQYFRVPGSKSTATISGLKPGV EYMIFVNAVTGSGAREEFSLPISINYRTEIDGGGGSGGGG SGGGGSGGGGSEYEARIEALIRAAQEQQEKNEAALRELD KWTGVWGNYEKV 415 >1,000 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWDAPAVTV RYYRITYGETGGNSPVQEFTVPGSKSTATISGLKPGVDYT ITVYAVTGRGESPASSKPISINYRTEIDGGGGSGGGGSGG GGSGGGGSRIEALIRAAQEQQEKNEAALRELFKWAS 416 >1,000 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWDAPAVTV RYYRITYGETGGNSPVQEFTVPGSKSTATISGLKPGVDYT ITVYAVTGRGESPASSKPISINYRTEIDGGGGSGGGGSGG GGSGGGGSRIEALIRAAQEQQQKNEAALRELDKWAS 417 428 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWDAPAVTV RYYRITYGETGGNSPVQEFTVPGSKSTATISGLKPGVDYT ITVYAVTGRGESPASSKPISINYRTEIDGGGGSGGGGSGG GGSGGGGSRIEALIRAAQEQQEKNEAALRELYKWAS 418 218 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWDAPAVTV RYYRITYGETGGNSPVQEFTVPGSKSTATISGLKPGVDYT ITVYAVTGRGESPASSKPISINYRTEIDGGGGSGGGGSGG GGSGGGGSRIEALIRAAQEQQEKNEAALRELLKWAS 419 >1,000 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWDAPAVTV RYYRITYGETGGNSPVQEFTVPGSKSTATISGLKPGVDYT ITVYAVTGRGESPASSKPISINYRTEIDGGGGSGGGGSGG GGSGGGGSRIEALIRAAQEQQEKNEAALRELQKWAS 420 8 MGHHHHHHGGSVSDVPRDLEVVAATPTSLLISWEYKVH PYRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGVD YTITVYAVTYGDDSAPISINYRTEIDGGGGSGGGGSGGG GSGGGGSRIEALIRAAQEQQEKNEAALRELDKWAS 421 50 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWVAGAED YQYYRITYGETGGNSPVQEFTVPHDLVTATISGLKPGVD YTITVYAVTDMMHVEYTEHPISINYRTEIDGGGGSGGGG SGGGGSGGAIAEYAARIEALIRAAQEQQEKNEAALRELD KWAS 422 3 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWKYKVHP YRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGVDY TITVYAVTYGVNSLPISINYRTEIDGGGGSGGGGSGGGGS GGGGTEYEARIEALIRAAQEQQEKNEAALRELDK 423 122 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWDAPAVTV RYYRITYGETGGNSPVQEFTVPGSKSTATISGLKPGVDYT ITVYAVTGRGESPASSKPISINYRTEIDGGGGSGGGGSGG GGSGGGGSRIEALIRAAQEQQEKNEAALRELYKWTS 424 39 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWDAPAVTV RYYRITYGETGGNSPVQEFTVPGSKSTATISGLKPGVDYT ITVYAVTGRGESPASSKPISINYRTEIDGGGGSGGGGSGG GGSGGGGSRIEALIRAAQEQQEKNEAALRELYKWASLWI 425 523 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWDAPAVTV RYYRITYGETGGNSPVQEFTVPGSKSTATISGLKPGVDYT ITVYAVTGRGESPASSKPISINYRTEIDGGGGSGGGGSGG GGSGGGGSRIEALIRAAQEQQEKNEAALRELYKWASRWN 426 139 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWDAPAVTV RYYRITYGETGGNSPVQEFTVPGSKSTATISGLKPGVDYT ITVYAVTGRGESPASSKPISINYRTEIDGGGGSGGGGSGG GGSGGGGSRIEALIRAAQEQQEKNEAALRELYKWASSWN 427 143 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWDAPAVTV RYYRITYGETGGNSPVQEFTVPGSKSTATISGLKPGVDYT ITVYAVTGRGESPASSKPISINYRTEIDGGGGSGGGGSGG GGSGGGGSRIEALIRAAQEQQEKNEAALRELYKWGS 428 50 MGHHHHHHGVSDVPRDLEVVAATPTSLLISWEYKVNN YRYYRITYGETGGNSPVQEFTVPSVLSTATISGLKPGVDY TITVYAVTVGVHSSPISINYRTEIDGGGGSGGGGSGGGGS GGGGSRIEALIRAAQEQQEKNEAALRELDK

In some embodiments, the anti-N17 Adnectin™-HIV fusion peptide inhibitor Combinectin or fusion proteins thereof comprise an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the non-linker regions of any one of SEQ ID NOs: 410-428.

In some embodiments, the anti-N17 Adnectin™-HIV fusion peptide inhibitor Combinectin or fusion proteins thereof comprise an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the non-linker regions of any one of SEQ ID NOs: 410-428, excluding any N-terminus extended region.

In other embodiments, anti-N17 Adnectin™-HIV fusion peptide inhibitor Combinectin comprises an anti-N17 Adnectin™ comprising an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the BC loop, DE loop and FG loop regions of SEQ ID NOs: 410-428.

In other embodiments, the anti-N17 Adnectin™-HIV fusion peptide inhibitor Combinectin comprises a HIV fusion peptide inhibitor comprising an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the HIV fusion peptide inhibitor of SEQ ID NOs: 410-428.

V. Anti-CD4 Adnectin™ Linked to an Anti-N17 Adnectin™ Linked to a HIV Fusion Peptide Inhibitor Combinectin

The anti-CD4 Adnectin™ linked to an anti-N17 Adnectin™ linked to a HIV fusion peptide inhibitor Combinectin of the invention include but are not limited to the following sequences:

Combinectin 3137 (SEQ ID NO: 3) GVSDVPRDLEVVAATPTSLLISWDAPAVTVHSYHIQYWPLGSYQRYQ VFSVPGSKSTATISGLKPGVEYQIRVYAETGRGESDQSLGWIQIGYR TE ESPEPETPEDE GVSDVPRDLEVVAATPTSLLISWQYKVHPYRYYR ITYGETGGNSPVQEFTVPSVLSTAEISGLKPGVDYTITVYAVTRGVD SAPISINYRTP GGGGSGGGGSGGGGSGGGG SEYEARIEALIRAAQEQ QEKNEAALRELYKWAL Combinectin 3151 (SEQ ID NO: 5) GVSDVPRDLEVVAATPTSLLISWDAPAVTVHSYHIQYWPLGSYQRYQ VFSVPGSKSTATISGLKPGVEYQIRVYAETGRGESDQSLGWIQIGYR TE ESPEPETPEDE GVSDVPRDLEVVAATPTSLLISWEYNVNPYRYYR ITYGETGGNSPVQEFTVPSVLSSAQISGLKPGVDYTITVYAVTRGVD SAPISINYRTP GGGGSGGGGSGGGGSGGGG SEYEARIEALIRAAQEQ QEKNEAALRELWKWAS Combinectin 3191 (SEQ ID NO: 7) GVSDVPRDLEVVAATPTSLLISWDAPAVTVHSYHIQYWPLGSYQRYQ VFSVPGSKSTATISGLKPGVEYQIRVYAETGRGESDQSLGWIQIGYR TP ESPEPETPEDE GVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYR ITYGETEGGNSPVQEFTVPSVLSSAEISGLKPGVDYTITVYAVTYGI DSPPISINYRTE GGGGSGGGGSGGGGSGGGG SEYEARIEALIRAAQE QQEKNEAALRELYKWAL Combinectin 3202 (SEQ ID NO: 9) GVSDVPRDLEVVAATPTSLLISWDAPAVTVHSYHIQYWPLGSYQRYQ VFSVPGSKSTATISGLKPGVEYQIRVYAETGGADSDQSFGWIQIGYR TP ESPEPETPEDE GVSDVPRDLEVVAATPTSLLISWEYKVHPYRYYR ITYGETGGNSPVQEFTVPSVLSTAEISGLKPGVDYTITVYAVTRGVD SAPISINYRTP GGGGSGGGGSGGGGSGGGG TIAEYAARIEALIRAAQ EQQEKNEAALRELYKWAS

In the sequences above, the anti-CD4 Adnectin™ sequences are underlined. The anti-N17 Adnectin™ sequences are double underlined. The HIV fusion peptide inhibitor sequences are underlined in bold. The linker sequences are italicized.

In some embodiments, the Combinectin or fusion proteins thereof comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 3, 5, 7 and 9.

In some embodiments, the Combinectin or fusion proteins thereof comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the non-linker regions of any one of SEQ ID NOs: 3, 5, 7 and 9.

In other embodiments, the Combinectin comprises an anti-CD4 Adnectin™ comprising an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the CD loop and FG loop regions of SEQ ID NOs: 3, 5, 7 and 9.

In other embodiments, the Combinectin comprises an anti-N17 Adnectin™ comprising an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the BC loop, DE loop and FG loop regions of SEQ ID NOs: 3, 5, 7 and 9.

In other embodiments, the Combinectin comprises a HIV fusion peptide inhibitor comprising an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the HIV fusion peptide inhibitor of SEQ ID NOs: 3, 5, 7 and 9.

VI. Pharmacokinetic Moieties

In one aspect, the application provides for an anti-CD4 moiety, an anti-gp41 moiety, a HIV fusion peptide inhibitor and combinations thereof further comprising a pharmacokinetic (PK) moiety. Improved pharmacokinetics may be assessed according to the perceived therapeutic need. Often it is desirable to increase bioavailability and/or increase the time between doses, possibly by increasing the time that a protein remains available in the serum after dosing. In some instances, it is desirable to improve the continuity of the serum concentration of the protein over time (e.g., decrease the difference in serum concentration of the protein shortly after administration and shortly before the next administration). The Combinectin of the invention may be attached to a moiety that reduces the clearance rate of the polypeptide in a mammal (e.g., mouse, rat, or human) by at least two-fold, at least 10-fold, at least 20-fold, at least 30-fold, at least 40-fold, at least 50-fold, at least 60-fold, at least 70-fold, at least 80-fold, at least 90-fold, at least 100-fold relative to the unmodified Combinectin. Other measures of improved pharmacokinetics may include serum half-life, which is often divided into an alpha phase and a beta phase. Either or both phases may be improved significantly by addition of an appropriate moiety. For example, the PK moiety may increase the serum half-life of the polypeptide by more than 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, 120%, 150%, 200%, 400%, 600%, 800%, 1000% or more relative to the Combinectin alone.

Moieties that slow clearance of a protein from the blood, herein referred to as “PK moieties”, include polyoxyalkylene moieties (e.g., polyethylene glycol), sugars (e.g., sialic acid), and well-tolerated protein moieties (e.g., Fc and fragments and variants thereof, transferrin, or serum albumin). The Combinectin of the invention may also be fused to albumin or a fragment (portion) or variant of albumin as described in U.S. Publication No. 2007/0048282, or may be fused to one or more Adnectins™ or other moieties that bind serum albumin, Fc, or transferrin.

Other PK moieties that can be used in the invention include those described in Kontermann et al., (Current Opinion in Biotechnology, 22:868-876 (2011)), herein incorporated by reference. Such PK moieties include, but are not limited to, human serum albumin fusions, human serum albumin conjugates, human serum albumin binders (e.g., Adnectin™ PKE, AlbudAb, ABD), XTEN fusions, PAS fusions (i.e., recombinant PEG mimetics based on the three amino acids proline, alanine, and serine), carbohydrate conjugates (e.g., hydroxyethyl starch (HES)), glycosylation, polysialic acid conjugates, and fatty acid conjugates.

Accordingly, in some embodiments the invention provides a Combinectin fused to a PK moiety that is a polymeric sugar. In some embodiments, the PK moiety is a polyethylene glycol moiety or an Fc region. In some embodiments the PK moiety is a serum albumin binding protein such as those described in U.S. Publication Nos. 2007/0178082 and 2007/0269422. In some embodiments the PK moiety is human serum albumin. In some embodiments, the PK moiety is transferrin.

The Fc fusion-Combinectin of the invention include the sequences shown in 3137 (SEQ ID NO: 4) and 3151 (SEQ ID NO: 6) of FIG. 2.

In some embodiments, the Fc fusion-Combinectin or fusion proteins thereof comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 4 and 6.

In some embodiments, the Fc fusion-Combinectin or fusion proteins thereof comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the non-linker regions of any one of SEQ ID NOs: 4 and 6.

In other embodiments, the Fc fusion-Combinectin comprises an anti-CD4 Adnectin™ comprising an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the CD loop and FG loop regions of SEQ ID NOs: 4 and 6.

In other embodiments, the Fc fusion-Combinectin comprises an anti-N17 Adnectin™ comprising an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the BC loop, DE loop and FG loop regions of SEQ ID NOs: 4 and 6.

In other embodiments, the Fc fusion-Combinectin comprises a fusion peptide inhibitor comprising an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the HIV fusion peptide inhibitor of SEQ ID NOs: 4 and 6.

The HSA fusion-Combinectin of the invention include the sequences shown in 3191 (SEQ ID NO: 8) and 3202 (SEQ ID NO: 10) of FIG. 2.

In some embodiments, the HSA fusion—Combinectin or fusion proteins thereof comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to any one of SEQ ID NOs: 8 and 10.

In some embodiments, the HSA fusion-Combinectin or fusion proteins thereof comprises an amino acid sequence at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the non-linker regions of any one of SEQ ID NOs: 8 and 10.

In other embodiments, the HSA fusion-Combinectin comprises an anti-CD4 Adnectin™ comprising an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the CD loop and FG loop regions of SEQ ID NOs: 8 and 10.

In other embodiments, the HSA fusion-Combinectin comprises an anti-N17 Adnectin™ comprising an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the BC loop, DE loop and FG loop regions of SEQ ID NOs: 8 and 10.

In other embodiments, the HSA fusion-Combinectin comprises a fusion peptide inhibitor comprising an amino acid sequence at least 80%, 85%, 90%, 95%, 98%, 99% or 100% identical to the HIV fusion peptide inhibitor of SEQ ID NOs: 8 and 10.

Polyethylene Glycol

In some embodiments, the anti-CD4 moiety, anti-gp41 moiety, HIV fusion peptide inhibitor and combinations thereof comprises polyethylene glycol (PEG). PEG is a well-known, water soluble polymer that is commercially available or can be prepared by ring-opening polymerization of ethylene glycol according to methods well known in the art (Sandler et al., Polymer Synthesis, Vol. 3, pp. 138-161, Academic Press, New York). The term “PEG” is used broadly to encompass any polyethylene glycol molecule, without regard to size or to modification at an end of the PEG, and can be represented by the formula: X—O(CH₂CH₂O)_(n-1)CH₂CH₂OH, where n is 20 to 2300 and X is H or a terminal modification, e.g., a C₁₋₄ alkyl. PEG can contain further chemical groups which are necessary for binding reactions, which result from the chemical synthesis of the molecule; or which act as a spacer for optimal distance of parts of the molecule. In addition, such a PEG can consist of one or more PEG side-chains which are linked together. PEGs with more than one PEG chain are called multiarmed or branched PEGs. Branched PEGs are described in, for example, European Published Application No. 473084A and U.S. Pat. No. 5,932,462.

One or more PEG molecules may be attached at different positions on the protein, and such attachment may be achieved by reaction with amines, thiols or other suitable reactive groups. The amine moiety may be, for example, a primary amine found at the N-terminus of a polypeptide or an amine group present in an amino acid, such as lysine or arginine. In some embodiments, the PEG moiety is attached at a position on the polypeptide selected from the group consisting of: a) the N-terminus; b) between the N-terminus and the most N-terminal beta strand or beta-like strand; c) a loop or strand residue positioned on a face of the polypeptide opposite the target-binding site; d) between the C-terminus and the most C-terminal beta strand or beta-like strand; e) within a linker sequence connecting two binding domains, and f) at the C-terminus.

PEGylation may be achieved by site-directed PEGylation, wherein a suitable reactive group is introduced into the protein to create a site where PEGylation preferentially occurs. In some embodiments, the protein is modified to introduce a cysteine residue at a desired position, permitting site-directed PEGylation on the cysteine. Mutations may be introduced into a protein coding sequence to generate cysteine residues. This might be achieved, for example, by mutating one or more amino acid residues to cysteine. Preferred amino acids for mutating to a cysteine residue include serine, threonine, alanine and other hydrophilic residues. Preferably, the residue to be mutated to cysteine is a surface-exposed residue. Algorithms are well-known in the art for predicting surface accessibility of residues based on primary sequence or a protein. Alternatively, surface residues may be predicted by comparing the amino acid sequences of binding polypeptides, given that the crystal structure of the framework, based on which binding polypeptides are designed and evolved, has been solved (see Himanen et al., Nature, 414:933-938 (2001)) and thus the surface-exposed residues identified. PEGylation of cysteine residues may be carried out using, for example, PEG-maleimide, PEG-vinylsulfone, PEG-iodoacetamide, or PEG-orthopyridyl disulfide.

The PEG is typically activated with a suitable activating group appropriate for coupling to a desired site on the polypeptide. PEGylation methods are well-known in the art and further described in Zalipsky, S. et al., “Use of Functionalized Poly(Ethylene Glycols) for Modification of Polypeptides” in Harris, J. M., Polyethylene Glycol Chemistry: Biotechnical and Biomedical Applications, Plenus Press, New York (1992), and in Zalipsky, Advanced Drug Reviews, 16:157-182 (1995).

PEG may vary widely in molecular weight and may be branched or linear. Typically, the weight-average molecular weight of PEG is from about 100 Daltons to about 150,000 Daltons. Exemplary weight-average molecular weights for PEG include about 20,000 Daltons, about 40,000 Daltons, about 60,000 Daltons and about 80,000 Daltons. In certain embodiments, the molecular weight of PEG is 40,000 Daltons. Branched versions of PEG having a total molecular weight of any of the foregoing can also be used. In some embodiments, the PEG has two branches. In other embodiments, the PEG has four branches. In another embodiment, the PEG is a bis-PEG (NOF Corporation, DE-200MA), to which two Adnectins™ are conjugated.

Conventional separation and purification techniques known in the art can be used to purify PEGylated Adnectin™, such as size exclusion (e.g., gel filtration) and ion exchange chromatography. Products may also be separated using SDS-PAGE. Products that may be separated include mono-, di-, tri-, poly- and un-PEGylated Adnectins™, as well as free PEG. The percentage of mono-PEG conjugates can be controlled by pooling broader fractions around the elution peak to increase the percentage of mono-PEG in the composition. About 90% mono-PEG conjugates represent a good balance of yield and activity.

In some embodiments, the PEGylated anti-CD4 moiety, anti-gp41 moiety, HIV fusion peptide inhibitor and combinations thereof will preferably retain at least about 25%, 50%, 60%, 70%, 80%, 85%, 90%, 95% or 100% of the biological activity associated with the unmodified anti-CD4 moiety, anti-gp41 moiety, Adnectin™ or Combinectin. In some embodiments, biological activity refers to its ability to bind to CD4 or gp41, as assessed by K_(d), k_(on), or k_(off). In some embodiments, the PEGylated anti-CD4 moiety, anti-gp41 moiety, Adnectin™ or Combinectin thereof shows an increase in binding to CD4 or gp41 relative to unPEGylated anti-CD4 moiety, anti-gp41 moiety, Adnectin™ or Combinectin.

Immunoglobulin Fc Domain (and Fragments)

In some embodiments, the peptide of the invention is fused to an immunoglobulin Fc domain, or a fragment or variant thereof. As used herein, a “functional Fc region” is an Fc domain or fragment thereof which retains the ability to bind FcRn. In some embodiments, a functional Fc region binds to FcRn, but does not possess effector functions. The ability of the Fc region or fragment thereof to bind to FcRn can be determined by standard binding assays known in the art. In other embodiments, the Fc region or fragment thereof binds to FcRn and possesses at least one “effector function” of a native Fc region. Exemplary “effector functions” include C1q binding; complement dependent cytotoxicity (CDC); Fc receptor binding; antibody-dependent cell-mediated cytotoxicity (ADCC); phagocytosis; down regulation of cell surface receptors (e.g., B cell receptor; BCR), etc. Such effector functions generally require the Fc region to be combined with a binding domain (e.g., an anti-CD4 or ant-N-17 Adnectin™) and can be assessed using various assays known in the art for evaluating such antibody effector functions.

A “native sequence Fc region” comprises an amino acid sequence identical to the amino acid sequence of an Fc region found in nature. A “variant Fc region” comprises an amino acid sequence which differs from that of a native sequence Fc region by virtue of at least one amino acid modification. Preferably, the variant Fc region has at least one amino acid substitution compared to a native sequence Fc region or to the Fc region of a parent polypeptide, e.g., from about one to about ten amino acid substitutions, and preferably from about one to about five amino acid substitutions in a native sequence Fc region or in the Fc region of the parent polypeptide. The variant Fc region herein will preferably possess at least about 80% sequence identity with a native sequence Fc region and/or with an Fc region of a parent polypeptide, and most preferably at least about 90% sequence identity therewith, more preferably at least about 95% sequence identity therewith.

In an exemplary embodiment, the Fc domain is derived from an IgG1 subclass, however, other subclasses (e.g., IgG2, IgG3, and IgG4) may also be used. Shown below is the sequence of a human IgG1 immunoglobulin Fc domain:

(SEQ ID NO: 11) DKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVS HEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWL NGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKN QVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYS KLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

The core hinge sequence is underlined, and the CH2 and CH3 regions are in regular text. It should be understood that the C-terminal glycine and lysine are optional in the Combinectin of the invention.

The fusion may be formed by attaching an Adnectin™ of the invention to either end of the Fc molecule, i.e., Fc-Adnectin™ or Adnectin™-Fc arrangements. In certain embodiments, the Fc and Adnectin™ are fused via a linker.

In some embodiments, the Fc region used in the Adnectin™ fusion comprises the hinge region of an Fc molecule. As used herein, the “hinge” region comprises the core hinge residues spanning positions 1-16 of SEQ ID NO: 11 (DKTHTCPPCPAPELLG; SEQ ID NO: 12) of the IgG1 Fc region. In certain embodiments, the Adnectin™-Fc fusion adopts a multimeric structure (e.g., dimer) owing, in part, to the cysteine residues at positions 6 and 9 of SEQ ID NO: 11 within the hinge region.

In certain embodiments, an Adnectin-Fc fusion may have the following configurations: 1) Adnectin™-hinge-Fc or 2) hinge-Fc-Adnectin™. Therefore, any Adnectin™ of the present invention can be fused to an Fc region comprising a hinge sequence according to these configurations. In some embodiments, a linker may be used to join the Adnectin™ to the hinge-Fc moiety, for example, an exemplary fusion protein may have the configuration Adnectin™-linker-hinge-Fc or hinge-Fc-linker-Adnectin™ Additionally, depending on the system in which the fusion polypeptide is produced, a leader sequence may be placed at the N-terminus of the fusion polypeptide. For example, if the fusion is produced in a mammalian system, a leader sequence may be added to the N-terminus of the fusion molecule. If the fusion is produced in E. coli, the fusion sequence will be preceded by a methionine.

VII. Nucleic Acid-Protein Fusion Technology

In one aspect, the invention provides an Adnectin™ comprising fibronectin type III domains that binds CD4 or the n17 domain of gp41. One way to rapidly make and test Fn3 domains with specific binding properties is the nucleic acid-protein fusion technology. This disclosure utilizes the in vitro expression and tagging technology, termed ‘PROfusion’ which exploits nucleic acid-protein fusions (RNA- and DNA-protein fusions) to identify novel polypeptides and amino acid motifs that are important for binding to proteins. Nucleic acid-protein fusion technology is a technology that covalently couples a protein to its encoding genetic information. For a detailed description of the RNA-protein fusion technology and fibronectin-based scaffold protein library screening methods see Szostak et al., U.S. Pat. Nos. 6,258,558, 6,261,804, 6,214,553, 6,281,344, 6,207,446, 6,518,018 and 6,818,418; Roberts et al., Proc. Natl. Acad. Sci., 94:12297-12302 (1997); and Kurz et al., Molecules, 5:1259-1264 (2000), all of which are herein incorporated by reference.

VIII. Vectors and Polynucleotides

Nucleic acids encoding any of the various proteins or polypeptides disclosed herein may be synthesized chemically. Codon usage may be selected so as to improve expression in a cell. Such codon usage will depend on the cell type selected. Specialized codon usage patterns have been developed for E. coli and other bacteria, as well as mammalian cells, plant cells, yeast cells and insect cells. See, for example, Mayfield et al., Proc. Natl. Acad. Sci. USA, 100(2):438-442 (Jan. 21, 2003); Sinclair et al., Protein Expr. Purif., 26(I):96-105 (October 2002); Connell, N. D., Curr. Opin. Biotechnol., 12(5):446-449 (October 2001); Makrides et al., Microbiol. Rev., 60(3):512-538 (September 1996); and Sharp et al., Yeast, 7(7):657-678 (October 1991).

General techniques for nucleic acid manipulation are described in, for example, Sambrook et al., Molecular Cloning: A Laboratory Manual, Second Edition, Vols. 1-3, Cold Spring Harbor Laboratory Press (1989), or Ausubel, F. et al., Current Protocols in Molecular Biology, Green Publishing and Wiley-Interscience, New York (1987) and periodic updates, herein incorporated by reference. Generally, the DNA encoding the polypeptide is operably linked to suitable transcriptional or translational regulatory elements derived from mammalian, viral, or insect genes. Such regulatory elements include a transcriptional promoter, an optional operator sequence to control transcription, a sequence encoding suitable mRNA ribosomal binding site, and sequences that control the termination of transcription and translation. The ability to replicate in a host, usually conferred by an origin of replication, and a selection gene to facilitate recognition of transformants is additionally incorporated.

The proteins described herein may be produced recombinantly not only directly, but also as a fusion polypeptide with a heterologous polypeptide, which is preferably a signal sequence or other polypeptide having a specific cleavage site at the N-terminus of the mature protein or polypeptide. The heterologous signal sequence selected preferably is one that is recognized and processed (i.e., cleaved by a signal peptidase) by the host cell.

For prokaryotic host cells that do not recognize and process a native signal sequence, the signal sequence is substituted by a prokaryotic signal sequence selected, for example, from the group of the alkaline phosphatase, penicillinase, 1 pp, or heat-stable enterotoxin II leaders.

For yeast secretion the native signal sequence may be substituted by, e.g., a yeast invertase leader, a factor leader (including Saccharomyces and Kluyveromyces alpha-factor leaders), or acid phosphatase leader, the C. albicans glucoamylase leader, or the signal sequence described in U.S. Pat. No. 5,631,144. In mammalian cell expression, mammalian signal sequences as well as viral secretory leaders, for example, the herpes simplex gD signal, are available. The DNA for such precursor regions may be ligated in reading frame to DNA encoding the protein.

Both expression and cloning vectors contain a nucleic acid sequence that enables the vector to replicate in one or more selected host cells. Generally, in cloning vectors this sequence is one that enables the vector to replicate independently of the host chromosomal DNA, and includes origins of replication or autonomously replicating sequences. Such sequences are well known for a variety of bacteria, yeast, and viruses. The origin of replication from the plasmid pBR322 is suitable for most Gram-negative bacteria, the 2 micron plasmid origin is suitable for yeast, and various viral origins (SV40, polyoma, adenovirus, VSV or BPV) are useful for cloning vectors in mammalian cells. Generally, the origin of replication component is not needed for mammalian expression vectors (the SV40 origin may typically be used only because it contains the early promoter).

Expression and cloning vectors may contain a selection gene, also termed a selectable marker. Typical selection genes encode proteins that (a) confer resistance to antibiotics or other toxins, e.g., ampicillin, neomycin, methotrexate, or tracycline, (b) complement auxotrophic deficiencies, or (c) supply critical nutrients not available from complex media, e.g., the gene encoding D-alanine racemase for Bacilli.

Expression and cloning vectors usually contain a promoter that is recognized by the host organism and is operably linked to the nucleic acid encoding the protein of the invention, e.g., a fibronectin-based scaffold protein. Promoters suitable for use with prokaryotic hosts include the phoA promoter, beta-lactamase and lactose promoter systems, alkaline phosphatase, a tryptophan (trp) promoter system, and hybrid promoters such as the tan promoter. However, other known bacterial promoters are suitable. Promoters for use in bacterial systems also will contain a Shine-Dalgarno (S.D.) sequence operably linked to the DNA encoding the protein of the invention. Promoter sequences are known for eukaryotes. Virtually all eukaryotic genes have an AT-rich region located approximately 25 to 30 bases upstream from the site where transcription is initiated. Another sequence found 70 to 80 bases upstream from the start of transcription of many genes is a CNCAAT region where N may be any nucleotide. At the 3′ end of most eukaryotic genes is an AATAAA sequence that may be the signal for addition of the poly A tail to the 3′ end of the coding sequence. All of these sequences are suitably inserted into eukaryotic expression vectors.

Examples of suitable promoting sequences for use with yeast hosts include the promoters for 3-phosphoglycerate kinase or other glycolytic enzymes, such as enolase, glyceraldehyde-3-phosphate dehydrogenase, hexokinase, pyruvate decarboxylase, phosphofructokinase, glucose-6-phosphate isomerase, 3-phosphoglycerate mutase, pyruvate kinase, triosephosphate isomerase, phosphoglucose isomerase, and glucokinase.

Transcription from vectors in mammalian host cells can be controlled, for example, by promoters obtained from the genomes of viruses such as polyoma virus, fowlpox virus, adenovirus (such as Adenovirus 2), bovine papilloma virus, avian sarcoma virus, cytomegalovirus, a retrovirus, hepatitis-B virus and most preferably Simian Virus 40 (SV40), from heterologous mammalian promoters, e.g., the actin promoter or an immunoglobulin promoter, from heat-shock promoters, provided such promoters are compatible with the host cell systems.

Transcription of a DNA encoding protein of the invention by higher eukaryotes is often increased by inserting an enhancer sequence into the vector. Many enhancer sequences are now known from mammalian genes (globin, elastase, albumin, α-fetoprotein, and insulin). Typically, however, one will use an enhancer from a eukaryotic cell virus. Examples include the SV40 enhancer on the late side of the replication origin (bp 100-270), the cytomegalovirus early promoter enhancer, the polyoma enhancer on the late side of the replication origin, and adenovirus enhancers. See also Yaniv, Nature, 297:17-18 (1982) on enhancing elements for activation of eukaryotic promoters. The enhancer may be spliced into the vector at a position 5′ or 3′ to the peptide-encoding sequence, but is preferably located at a site 5′ from the promoter.

Expression vectors used in eukaryotic host cells (e.g., yeast, fungi, insect, plant, animal, human, or nucleated cells from other multicellular organisms) will also contain sequences necessary for the termination of transcription and for stabilizing the mRNA. Such sequences are commonly available from the 5′ and, occasionally 3′, untranslated regions of eukaryotic or viral DNAs or cDNAs. These regions contain nucleotide segments transcribed as polyadenylated fragments in the untranslated portion of mRNA encoding the protein of the invention. One useful transcription termination component is the bovine growth hormone polyadenylation region. See WO 94/11026 and the expression vector disclosed therein.

The recombinant DNA can also include any type of protein tag sequence that may be useful for purifying the protein. Examples of protein tags include, but are not limited to, a histidine tag, a FLAG tag, a myc tag, an HA tag, or a GST tag. Appropriate cloning and expression vectors for use with bacterial, fungal, yeast, and mammalian cellular hosts can be found in Cloning Vectors: A Laboratory Manual, Elsevier, New York (1985), the relevant disclosure of which is hereby incorporated by reference.

The expression construct is introduced into the host cell using a method appropriate to the host cell, as will be apparent to one of skill in the art. A variety of methods for introducing nucleic acids into host cells are known in the art, including, but not limited to, electroporation; transfection employing calcium chloride, rubidium chloride, calcium phosphate, DEAE-dextran, or other substances; microprojectile bombardment; lipofection; and infection (where the vector is an infectious agent).

Suitable host cells include prokaryotes, yeast, mammalian cells, or bacterial cells. Suitable bacteria include gram negative or gram positive organisms, for example, E. coli or Bacillus spp. Yeast, preferably from the Saccharomyces species, such as S. cerevisiae, may also be used for production of polypeptides. Various mammalian or insect cell culture systems can also be employed to express recombinant proteins. Baculovirus systems for production of heterologous proteins in insect cells are reviewed by Luckow et al. (Bio/Technology, 6:47 (1988)). Examples of suitable mammalian host cell lines include endothelial cells, COS-7 monkey kidney cells, CV-1, L cells, C127, 3T3, Chinese hamster ovary (CHO), human embryonic kidney cells, HeLa, 293, 293T, and BHK cell lines. Purified polypeptides are prepared by culturing suitable host/vector systems to express the recombinant proteins. For many applications, the small size of many of the polypeptides disclosed herein would make expression in E. coli as the preferred method for expression. The protein is then purified from culture media or cell extracts.

IX. Protein Production

The present invention is also directed to cell lines that express a Combinectin or fusion protein thereof. Creation and isolation of cell lines producing a Combinectin can be accomplished using standard techniques known in the art, such as those described herein.

Host cells are transformed with the herein-described expression or cloning vectors for protein production and cultured in conventional nutrient media modified as appropriate for inducing promoters, selecting transformants, or amplifying the genes encoding the desired sequences. In the examples shown here, the host cells used for high-throughput protein production (HTPP) and mid-scale production were those from the HMS174-bacterial strain.

The host cells used to produce the proteins of this invention may be cultured in a variety of media. Commercially available media such as Ham's F10 (Sigma), Minimal Essential Medium ((MEM), (Sigma), RPMI-1640 (Sigma), and Dulbecco's Modified Eagle's Medium ((DMEM), Sigma)) are suitable for culturing the host cells. In addition, many of the media described in Ham et al., Meth. Enzymol., 58:44 (1979), Barites et al., Anal. Biochem., 102:255 (1980), U.S. Pat. Nos. 4,767,704, 4,657,866, 4,927,762, 4,560,655, 5,122,469, 6,048,728, 5,672,502, or U.S. Patent No. RE 30,985 may be used as culture media for the host cells. Any of these media may be supplemented as necessary with hormones and/or other growth factors (such as insulin, transferrin, or epidermal growth factor), salts (such as sodium chloride, calcium, magnesium, and phosphate), buffers (such as HEPES), nucleotides (such as adenosine and thymidine), antibiotics (such as Gentamycin drug), trace elements (defined as inorganic compounds usually present at final concentrations in the micromolar range), and glucose or an equivalent energy source. Any other necessary supplements may also be included at appropriate concentrations that would be known to those skilled in the art. The culture conditions, such as temperature, pH, and the like, are those previously used with the host cell selected for expression, and will be apparent to the ordinarily skilled artisan.

Proteins disclosed herein can also be produced using cell-free translation systems. For such purposes the nucleic acids encoding the polypeptide must be modified to allow in vitro transcription to produce mRNA and to allow cell-free translation of the mRNA in the particular cell-free system being utilized (eukaryotic such as a mammalian or yeast cell-free translation system or prokaryotic such as a bacterial cell-free translation system.

Proteins of the invention can also be produced by chemical synthesis (e.g., by the methods described in Solid Phase Peptide Synthesis, Second Edition, The Pierce Chemical Co., Rockford, Ill. (1984)). Modifications to the protein can also be produced by chemical synthesis.

The proteins of the present invention can be purified by isolation/purification methods for proteins generally known in the field of protein chemistry. Non-limiting examples include extraction, recrystallization, salting out (e.g., with ammonium sulfate or sodium sulfate), centrifugation, dialysis, ultrafiltration, adsorption chromatography, ion exchange chromatography, hydrophobic chromatography, normal phase chromatography, reversed-phase chromatography, get filtration, gel permeation chromatography, affinity chromatography, electrophoresis, countercurrent distribution or any combinations of these. After purification, polypeptides may be exchanged into different buffers and/or concentrated by any of a variety of methods known to the art, including, but not limited to, filtration and dialysis.

The purified polypeptide is preferably at least 85% pure, or preferably at least 95% pure, and most preferably at least 98% pure. Regardless of the exact numerical value of the purity, the polypeptide is sufficiently pure for use as a pharmaceutical product.

X. Biophysical and Biochemical Characterization

Binding of the protein of the invention to a target molecule (e.g., CD4 or gp41) may be assessed in terms of equilibrium constants (e.g., dissociation, K_(d)) and in terms of kinetic constants (e.g., on-rate constant, k_(on) and off-rate constant, k_(off)). The protein of the invention will generally bind to a target molecule with a K_(d) of less than 500 nM, 100 nM, 10 nM, 1 nM, 500 pM, 200 pM, or 100 pM, although higher K_(d) values may be tolerated where the k_(off) is sufficiently low or the k_(on), is sufficiently high.

In Vitro Assays for Binding Affinity

Proteins that bind CD4 or gp41 can be identified using various in vitro assays. Preferably, the assays are high-throughput assays that allow for screening multiple candidates simultaneously.

In some embodiments, biomolecular interactions can be monitored in real time with the BIACORE® system, which uses SPR to detect changes in the resonance angle of light at the surface of a thin gold film on a glass support due to changes in the refractive index of the surface up to 300 nm away. BIACORE® analysis generates association rate constants, dissociation rate constants, equilibrium dissociation constants, and affinity constants. Binding affinity is obtained by assessing the association and dissociation rate constants using a BIACORE® surface plasmon resonance system (Biacore, Inc.). A biosensor chip is activated for covalent coupling of the target. The target is then diluted and injected over the chip to obtain a signal in response units of immobilized material. Since the signal in resonance units (RU) is proportional to the mass of immobilized material, this represents a range of immobilized target densities on the matrix. Association and dissociation data are fit simultaneously in a global analysis to solve the net rate expression for a 1:1 bimolecular interaction, yielding best fit values for k_(on), k_(off) and R_(max) (maximal response at saturation). Equilibrium dissociation constants for binding, K_(d)'s are calculated from SPR measurements as k_(off)/k_(on).

In some embodiments, the Combinectin of the invention exhibit a K_(d) of 100 nM or less. Preferably, the K_(d) is 10 nM or less. More preferably, the K_(d) is 1 nM or less.

In some embodiments, the Combinectin of the invention exhibit an IC₅₀ of 5 nM or less, 4 nM or less, 3 nM or less, 2.5 nM or less, 2 nM or less, 1.5 nM or less, 1 nM or less, 0.5 nM or less, 0.2 nM or less, or 0.1 nM or less. Preferably, the IC₅₀ is 1.5 nM or less. More preferably, the IC₅₀ is 0.5 nM or less.

It should be understood that the assays described herein above are exemplary, and that any method known in the art for determining the binding affinity between proteins (e.g., fluorescence based-transfer (FRET), enzyme-linked immunosorbent assay, and competitive binding assays (e.g., radioimmunoassays)) can be used to assess the binding affinities of the Combinectin of the invention.

In the present invention, ELISA assays were utilized for identifying Adnectins™ that bind to CD4 or gp41, with affinities determined by BIACORE® SPR. FACS assays were also used to determine the EC₅₀ of binding of the CD4 Adnectin™ (alone and as part of the full Combinectin) to CD4 as presented naturally on T-cell surfaces. Peptide affinities were measured by BIACORE® SPR.

As described in Table 5 below, the range of binding affinities (by SPR) for CD4 Adnectins™ to CD4 was 0.3 nM to 140 nM; the range for N17 Adnectin™ binding to artificial gp41-based targets was 0.5 nM to 40 nM; the range for peptide binding was 0.2 nM to 70 nM. SPR-based affinities for the Combinectin of the invention and for the individual components thereof are shown in Table 5 below.

TABLE 5 Binding Affinities for Combinectin and Individual Components K_(on) K_(off) K_(d) Protein ID Target (1/Ms) (1/s) (nM) CD4 ADX_ CD4 1.9E+05 7.6E−04 4 Adnectin ™ 6940_B01 N17 ADX_ gp41 7.0E+06 3.3E−03 0.5 Adnectin ™ 6200_A08 (IZN24) peptide 203613-24 gp41 2.3E+06 2.5E−04 0.1 (PRD-828) HSA- BMT- CD4 7.6E+03 8.3E−04 109 Combinectin 180280 HSA- BMT- gp41 8.1E+05 1.7E−03 2 Combinectin 180280 (IZN24) HSA- BMT- gp41 9.6E+05 1.8E−04 0.2 Combinectin 180280 (PRD-828) In Vitro Assays for Inhibition Activity

Various art-recognized in vitro systems exist that allow for examination of the potency of the Combinectin (or of individual inhibitors or combinations thereof) against HIV-1 infection. These include systems that allow for complete replication of laboratory-derived virus or clinical isolates of various strains in cultured cells or peripheral blood monocyte cultures. In addition, systems that recapitulate the early cell entry stages of infection, without using viable virus, could be used to analyze the effectiveness of the Combinectin, individual inhibitors or combinations thereof. These include, but are not limited to, “pseudotyped” viruses that contain deletions that make them unable to produce infectious virions or cells that express only the HIV gp160 gene that can be used to monitor the HIV-1specific fusion reaction to target cells.

In Vivo Models

One skilled in the art would know of various art-recognized animal models that allow for replication and in some cases recapitulate the symptoms of HIV infection. These models can be used to test the efficacy of the Combinectin, individual inhibitors or combinations thereof of the invention.

XI. Therapeutic Applications

In one aspect, the present invention provides Combinectins useful for the treatment of HIV. Accordingly, in certain embodiments the invention provides methods for attenuating or inhibiting HIV fusion in a subject comprising administering an effective amount of the Combinectin of the invention to a subject. In some embodiments, the subject is a human. In some embodiments, the Combinectin of the invention is pharmaceutically acceptable to a mammal, in particular a human. A “pharmaceutically acceptable” polypeptide refers to a polypeptide that is administered to an animal without significant adverse medical consequences.

In some embodiments, the Combinectin of the present invention will be administered to a subject in combination (concurrently or separately) with an agent known in the art to be useful for the particular disorder or disease being treated.

In some embodiments, the target patient population for Combinectin therapy is one that is not amenable to standard therapy for the disease being treated due to, e.g., age, pre-existing conditions, genetic makeup, and/or co-morbidities. The Combinectin of the invention can serve as an alternative to existing therapies that are associated with substantial side effects or safety concerns.

In some embodiments, the target patient population for Combinectin therapy is comprised of uninfected individuals at high risk of infection, due to lifestyle or other aggravating factors. The Combinectin is used to protect these individuals from getting infected by HIV (pre-exposure prophylaxis).

XII. Pharmaceutical Compositions

The present invention further provides pharmaceutical compositions comprising a Combinectin or fusion proteins thereof described herein, wherein the composition is essentially endotoxin free, or at least contain no more than acceptable levels of endotoxins as determined by the appropriate regulatory agency (e.g., FDA).

Compositions of the present invention can be in the form of a pill, tablet, capsule, liquid, or sustained release tablet for oral administration; a liquid for intravenous, subcutaneous or parenteral administration; or a gel, lotion, ointment, cream, or a polymer or other sustained release vehicle for local administration, or an atomizable suspension suitable for inhaled or intranasal administration.

Methods well known in the art for making compositions are found, for example, in Gennaro, A. R., ed., Remington: The Science and Practice of Pharmacy, 20th Edition, Lippincott Williams & Wilkins, Philadelphia, Pa. (2000). Compositions for parenteral administration may, for example, contain excipients, sterile water, saline, polyalkylene glycols such as polyethylene glycol, oils of vegetable origin, or hydrogenated naphthalenes. Biocompatible, biodegradable lactide polymer, lactide/glycolide copolymer, or polyoxyethylene-polyoxypropylene copolymers may be used to control the release of the compounds. Nanoparticulate compositions (e.g., biodegradable nanoparticles, solid lipid nanoparticles, liposomes) may be used to control the biodistribution of the compounds. Other potentially useful parenteral delivery systems include ethylene-vinyl acetate copolymer particles, osmotic pumps, implantable infusion systems, and liposomes. The concentration of the compound in the composition varies depending upon a number of factors, including the dosage of the drug to be administered, and the route of administration.

Acceptable carriers, excipients, or stabilizers are nontoxic to recipients at the dosages and concentrations employed, and include buffers such as phosphate, citrate, and other organic acids; antioxidants including ascorbic acid and methionine; preservatives (such as octadecyldimethylbenzyl ammonium chloride; hexamethonium chloride; benzalkonium chloride, benzethonium chloride; phenol, butyl or benzyl alcohol; alkyl parabens such as methyl or propyl paraben; catechol; resorcinol; cyclohexanol; 3-pentanol; and m-cresol); low molecular weight (less than about 10 residues) polypeptides; proteins, such as serum albumin, gelatin, or immunoglobulins; hydrophilic polymers such as polyvinylpyrrolidone; amino acids such as glycine, glutamine, asparagine, histidine, arginine, or lysine; monosaccharides, disaccharides, and other carbohydrates including glucose, mannose, or dextrans; chelating agents such as EDTA; sugars such as sucrose, mannitol, trehalose or sorbitol; salt-forming counter-ions such as sodium; metal complexes (e.g., Zn-protein complexes); and/or non-ionic surfactants such as Tween, PLURONIC® or polyethylene glycol (PEG).

The active ingredients may also be entrapped in a microcapsule prepared, for example, by coacervation techniques or by interfacial polymerization, for example, hydroxymethylcellulose or gelatin-microcapsule and poly-(methylmethacylate) microcapsule, respectively, in colloidal drug delivery systems (for example, liposomes, albumin microspheres, microemulsions, nano-particles and nanocapsules) or in macroemulsions. Such techniques are disclosed in Osol, A., ed., Remington's Pharmaceutical Sciences, 16th Edition (1980).

Sustained-release preparations may be prepared. Suitable examples of sustained-release preparations include semipermeable matrices of solid hydrophobic polymers containing the proteins of the invention, which matrices are in the form of shaped articles, e.g., films, or microcapsule. Examples of sustained-release matrices include polyesters, hydrogels (for example, poly(2-hydroxyethyl-methacrylate), or poly(vinylalcohol)), polylactides (U.S. Pat. No. 3,773,919), copolymers of L-glutamic acid and y ethyl-L-glutamate, non-degradable ethylene-vinyl acetate, degradable lactic acid-glycolic acid copolymers such as the LUPRON DEPOT® (injectable microspheres composed of lactic acid-glycolic acid copolymer and leuprolide acetate), and poly-D-(−)-3-hydroxybutyric acid. While polymers such as ethylene-vinyl acetate and lactic acid-glycolic acid enable release of molecules for over 100 days, certain hydrogels release proteins for shorter time periods. When encapsulated proteins of the invention may remain in the body for a long time, they may denature or aggregate as a result of exposure to moisture at 37° C., resulting in a loss of biological activity and possible changes in immunogenicity. Rational strategies can be devised for stabilization depending on the mechanism involved. For example, if the aggregation mechanism is discovered to be intermolecular S—S bond formation through thio-disulfide interchange, stabilization may be achieved by modifying sulfhydryl residues, lyophilizing from acidic solutions, controlling moisture content, using appropriate additives, and developing specific polymer matrix compositions.

Compositions of the present invention for oral use include tablets containing the active ingredient(s) in a mixture with non-toxic pharmaceutically acceptable excipients. These excipients may be, for example, inert diluents or fillers (e.g., sucrose and sorbitol), lubricating agents, glidants, and anti-adhesives (e.g., magnesium stearate, zinc stearate, stearic acid, silicas, hydrogenated vegetable oils, or talc). Compositions for oral use may also be provided as chewable tablets, or as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium.

The pharmaceutical composition to be used for in vivo administration typically must be sterile. This may be accomplished by filtration through sterile filtration membranes. Where the composition is lyophilized, sterilization using this method may be conducted either prior to or following lyophilization and reconstitution. The composition for parenteral administration may be stored in lyophilized form or in solution. In addition, parenteral compositions generally are placed into a container having a sterile access port, for example, an intravenous solution bag or vial having a stopper pierceable by a hypodermic injection needle.

Once the pharmaceutical composition has been formulated, it may be stored in sterile vials as a solution, suspension, gel, emulsion, solid, or a dehydrated or lyophilized powder. Such formulations may be stored either in a ready-to-use form or in a form (e.g., lyophilized) requiring reconstitution prior to administration.

The compositions herein may also contain more than one active compound as necessary for the particular indication being treated, preferably those with complementary activities that do not adversely affect each other. Such molecules are suitably present in combination in amounts that are effective for the purpose intended.

XIII. Administration

A pharmaceutical composition comprising a Combinectin or fusion protein thereof of the present invention can be administered to a subject with HIV using standard administration techniques including oral, parenteral, pulmonary, transdermal, intramuscular, intranasal, buccal, sublingual, or suppository administration. Preferably, administration of the Combinectins of the invention is parenteral. The term parenteral as used herein includes intravenous, intramuscular, subcutaneous, rectal, vaginal, or intraperitoneal administration. Peripheral systemic delivery by intravenous or intraperitoneal or subcutaneous injection is preferred.

A therapeutically effective dose refers to a dose that produces the therapeutic effects for which it is administered. An effective amount of a pharmaceutical composition to be employed therapeutically will depend, for example, upon the therapeutic context and objectives. One skilled in the art will appreciate that the appropriate dosage levels for treatment will thus vary depending, in part, upon the molecule delivered, the indication for which the binding agent molecule is being used, the route of administration, and the size (body weight, body surface or organ size) and condition (the age and general health) of the patient.

For example, the therapeutically effective dose can be estimated initially either in cell culture assays or in animal models such as mice, rats, rabbits, dogs, pigs, or monkeys. An animal model may also be used to determine the appropriate concentration range and route of administration. Such information can then be used to determine useful doses and routes for administration in humans.

The exact dosage will be determined in light of factors related to the subject requiring treatment, and may be ascertained using standard techniques. Dosage and administration are adjusted to provide sufficient levels of the active compound or to maintain the desired effect. Factors that may be taken into account include the severity of the disease state, the general health of the subject, the age, weight, and gender of the subject, time and frequency of administration, drug combination(s), reaction sensitivities, and response to therapy. In general, the Combinectin of the present invention are administered at about 0.01 mg/kg to about 50 mg/kg per day, preferably about 0.01 mg/kg to about 30 mg/kg per day, most preferably about 0.01 mg/kg to about 20 mg/kg per day. In some embodiments, the Combinectin of the present invention are administered at weekly dosages of about 0.01 mg/kg to about 10 mg/kg, more preferably about 0.01 to about 5 mg/kg, most preferably about 0.01 to about 1 mg/kg. Alternatively, the Combinectin of the invention are administered at about 15 to about 100 mg/week, from about 20 to about 80 mg/week, from about 20 to about 60 mg/week, or about 20 to about 25 mg/week.

The frequency of dosing will depend upon the pharmacokinetic parameters of the binding agent molecule in the formulation used. Typically, a composition is administered until a dosage is reached that achieves the desired effect. The composition may therefore be administered as a single dose or as multiple doses (at the same or different concentrations/dosages) over time, or as a continuous infusion. Further refinement of the appropriate dosage is routinely made. Appropriate dosages may be ascertained through use of appropriate dose-response data. For example, the Combinectin may be given daily (e.g., once, twice, three times, or four times daily) or less frequently (e.g., once every other day, once or twice weekly, or monthly). In addition, as is known in the art, adjustments for age as well as the body weight, general health, sex, diet, time of administration, drug interaction, and the severity of the disease may be necessary, and will be ascertainable with routine experimentation by those skilled in the art. The Combinectin is suitably administered to the patient at one time or over a series of treatments.

Administration of a Combinectin or a fusion thereof, and one or more additional therapeutic agents, whether co-administered or administered sequentially, may occur as described above for therapeutic applications. Suitable pharmaceutically acceptable carriers, diluents, and excipients for co-administration will be understood by the skilled artisan to depend on the identity of the particular therapeutic agent being administered.

XIV. Kits and Articles of Manufacture

The Combinectin of the invention can be provided in a kit, a packaged combination of reagents in predetermined amounts with instructions for use in the therapeutic or diagnostic methods of the invention.

For example, in one embodiment of the invention, an article of manufacture containing materials useful for the treatment or prevention of the disorders or conditions described above is provided. The article of manufacture comprises a container and a label. Suitable containers include, for example, bottles, vials, syringes, and test tubes. The containers may be formed from a variety of materials such as glass or plastic. The container holds a composition of the invention which is effective for treating HIV and may have a sterile access port (for example, the container may be an intravenous solution bag or a vial having a stopper pierceable by a hypodermic injection needle). The active agent in the composition is a Combinectin of the invention. The label on, or associated with, the container indicates that the composition is used for treating HIV. The article of manufacture may further comprise a second container comprising a pharmaceutically-acceptable buffer, such as phosphate-buffered saline, Ringer's solution and dextrose solution. It may further include other materials desirable from a commercial and user standpoint, including other buffers, diluents, filters, needles, syringes, and package inserts with instructions for use.

INCORPORATION BY REFERENCE

All documents and references, including patent documents and websites, described herein are individually incorporated by reference to into this document to the same extent as if there were written in this document in full or in part.

The invention is now described by reference to the following examples, which are illustrative only, and are not intended to limit the present invention. While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one of skill in the art that various changes and modifications can be made thereto without departing from the spirit and scope thereof.

EXAMPLES Example 1—Combinectin Production/Purification

HIV Combinectin Tandem—Bacterial

Transformed DNA into BL21(DE3) bacterial cells.

Cells grown up in bacterial culture at ˜37° C. to a target OD₆₀₀

Culture temperature dropped to ˜30° C., and culture is induced with IPTG and harvested after several hours.

Harvest is performed using a centrifuge.

Recovery of protein is performed using a chemical lysis and a MICROFLUIDIZER®, followed by clarification by centrifugation or tangential flow filtration. Lysate is processed immediately or frozen for later use.

Purification by Hydrophobic Interaction Chromatography followed by hydroxyapatite chromatography and/or ion exchange chromatography. Formulated and concentrated using tangential flow filtration.

HIV Combinectin-Fc Construct; Mammalian Cell Culture

DNA is transfected into appropriate mammalian cells.

Cells grown in cell culture.

Harvested by centrifugation and/or filtration.

Purification using affinity chromatography and ion exchange chromatography.

Formulated and concentrated using tangential flow filtration.

HIV Combinectin-HuSA construct; Mammalian Cell Culture

DNA is transfected into appropriate mammalian cells.

Cells grown in cell culture.

Harvested by centrifugation and/or filtration.

Purification by Hydrophobic Interaction Chromatography followed by hydroxyapatite chromatography and/or ion exchange chromatography.

Formulated and concentrated using tangential flow filtration.

Example 2—Combinectin Potency Assay

MT-2 cells, HEK 293T cells and the proviral DNA clone of NU-3 were obtained from the NIH AIDS Research and Reference Reagent Program. MT-2 cells were propagated in RPMI 1640 medium supplemented with 10% heat-inactivated fetal bovine serum (FBS), 10 mM HEPES buffer pH 7.55, and 2 mM L-glutamine. HEK 293T cells were propagated in DMEM media supplemented with 10% heat-inactivated FBS, 10 mM HEPES buffer pH 7.55 and 2 mM L-glutamine. Recombinant NL-Rluc virus, in which a section of the nef gene from the proviral clone of NL₄₋₃ was replaced with the Renilla luciferase gene, was constructed at Bristol-Myers Squibb. The replication-competent virus was harvested 3 days after transfection of HEK 293T cells with the modified pNL-Rluc proviral clone. Transfections were performed using Lipofectamine Plus (Invitrogen, Carlsbad, Calif.), according to manufacturer's instruction. Virus was titered in MT-2 cells using luciferase enzyme activity as a biomarker. The NL-Rluc virus used to infect MT-2 cells a multiplicity of 0.01 for 1 hour before adding to the peptides in 96-well plates. Peptides were serially diluted three-fold and 11 concentrations were plated in triplicate. After 4-5 days of incubation, cells were processed and quantitated for virus growth by the amount of expressed luciferase. Luciferase was quantitated using the Dual Luciferase kit from Promega (Madison, Wis.), with modifications to the manufacturer's protocol. The diluted Passive Lysis solution was pre-mixed with the re-suspended Luciferase Assay Reagent and then re-suspended in STOP & GLO® Substrate (2:1:1 ratio). A total of 50 pt of the mixture was added to each aspirated well on assay plates and luciferase activity was measured immediately on a Wallac TriLux (Perkin-Elmer, Waltham, Mass.). The 50% effective concentration (EC₅₀) was calculated by comparing the amount of luciferase produced in the presence of inhibitory peptide compared to wells where no peptide was added.

Example 3—Evaluation of Combinectin Pharmacokinetics

Human CD4 Transgenic Mouse Model

Male and female heterozygous human CD4 mice were obtained from Jackson Laboratories, Bar Harbor, Me.

WT Mouse PK Studies

8-21 day single IV bolus dose studies were run in female C57Bl/6 WT mice to assess the PK properties of the various Combinectins. Fc-Combinectin fusions were dosed at 10 mg/kg and HSA-Combinectin fusions were dosed at 8.8 mg/kg. Plasma samples were collected in CPD and stored at −80° C. until analysis.

hCD4 Mouse PK Studies

7-10 day single IV bolus dose studies were run in heterozygous hCD4 mice to assess the PK properties of various Combinectins in the presence of target. Combinectins doses and sample collection methods were the same as described above for the WT mice.

Cynomolgus Monkey Studies

A 1-week single dose study was conducted in female cynos to determine the PK of Combinectins. Following a 1 mg/kg dose, serum samples were collected at the indicated times, aliquoted and quick frozen for MSD or LC/MS analysis.

Pharmacokinetic Measurements

Drug levels were measured in mouse or cyno plasma using the Mesoscale technology platform or colorimetric ELISA formats. Fc-Combinectin fusions were captured via the protein PRD828 (BMS) that specifically binds the peptide component of Combinectins and detected using a Goat anti-Human IgG Fc-HRP conjugated pAb (Pierce #31413). HSA-Combinectin fusions were captured via PRD828 and detected using a goat pAb against HSA (Bethyl, TX #A80-229A) that was ruthenium labeled. Sample concentrations were calculated from a standard curve using a 5-parameter logarithmic fit. Non-compartmental analyses were performed using Phoenix WINNONLIN® 6.3 (Pharsight Corporation, Mountain View, Calif.) using a plasma model and linear up/log down calculation method. 

We claim:
 1. A polypeptide comprising two active domains, wherein one domain is a fibronectin-based scaffold domain protein that binds the N17 domain of glycoprotein 41 (gp41) and comprises the amino acid sequence that is at least 90% identical to the amino acid sequence of any one of SEQ ID NOs: 115-371; and the other domain is a cluster of differentiation 4 (CD4) binding moiety or a human immunodeficiency virus (HIV) fusion peptide inhibitor, wherein the CD4 binding moiety is selected from the group consisting of an anti-CD4 antibody or fragment thereof, and a fibronectin-based scaffold domain protein that binds CD4 and comprises the amino acid sequence that is at least 90% identical to the amino acid sequence of any one of SEQ ID NOs: 95-114.
 2. The polypeptide of claim 1, wherein the two domains are connected to each other in any order by linkers.
 3. The polypeptide of claim 1, further comprising one or more pharmacokinetic (PK) moieties selected from the group consisting of polyethylene glycol, sialic acid, Fc, Fc fragment, transferrin, serum albumin, a serum albumin binding protein, and a serum immunoglobulin binding protein.
 4. The polypeptide of claim 3, wherein the PK moiety is Fc.
 5. The polypeptide of claim 4, wherein the Fc is attached to the N-terminus of the polypeptide.
 6. The polypeptide of claim 3, wherein the PK moiety is human serum albumin.
 7. The polypeptide of claim 6, wherein the human serum albumin is attached to the N-terminus of the polypeptide. 